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Details of SAPdb entry with Sequence FF

Primary information
SAPdb ID	1001,
PMID	18070345
Peptide Name	Fmoc-Phe-Phe
Peptide sequence	FF
N-Terminal Modification	Fmoc
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	Confocal Microscopy
Solvent	Dispersion medium= PBS 10x, DMSO (gelling agent)= 100mg/ml
Method	Lyophilized Fmoc-Phe-Phe dipeptide was weighed and dissolved in DMSO. This was applied to the desired dispersion medium.
Conc	0.005%
Temperature	pH 7
Temperature	37 °C
Year	2007
Self assembly	No
Type of Self assembly	Unstable hydrogel assembly
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Unstable
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1002,
PMID	18070345
Peptide Name	Fmoc-Phe-Phe
Peptide sequence	FF
N-Terminal Modification	Fmoc
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	Confocal Microscopy
Solvent	Dispersion medium= PBS 1x, DMSO (gelling agent)= 100mg/ml
Method	Lyophilized Fmoc-Phe-Phe dipeptide was weighed and dissolved in DMSO. This was applied to the desired dispersion medium.
Conc	0.005%
Temperature	pH 7
Temperature	37 °C
Year	2007
Self assembly	No
Type of Self assembly	Unstable hydrogel assembly
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Unstable
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1003,
PMID	18070345
Peptide Name	Fmoc-Phe-Phe
Peptide sequence	FF
N-Terminal Modification	Fmoc
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	Confocal Microscopy
Solvent	Dispersion medium= PBS 1x, DMSO (gelling agent)= 100mg/ml
Method	Lyophilized Fmoc-Phe-Phe dipeptide was weighed and dissolved in DMSO. This was applied to the desired dispersion medium.
Conc	0.01%
Temperature	pH 7
Temperature	37 °C
Year	2007
Self assembly	No
Type of Self assembly	Partial hydrogel assembly
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Partial
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1004,
PMID	18070345
Peptide Name	Fmoc-Phe-Phe
Peptide sequence	FF
N-Terminal Modification	Fmoc
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	Confocal Microscopy
Solvent	Dispersion medium= PBS 1x, DMSO (gelling agent)= 25mg/ml
Method	Lyophilized Fmoc-Phe-Phe dipeptide was weighed and dissolved in DMSO. This was applied to the desired dispersion medium.
Conc	0.005%
Temperature	pH 7
Temperature	37 °C
Year	2007
Self assembly	No
Type of Self assembly	Soft hydrogel assembly
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Soft gel
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1005,
PMID	18070345
Peptide Name	Fmoc-Phe-Phe
Peptide sequence	FF
N-Terminal Modification	Fmoc
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	Confocal Microscopy
Solvent	Dispersion medium= PBS 1x, DMSO (gelling agent)= 25mg/ml
Method	Lyophilized Fmoc-Phe-Phe dipeptide was weighed and dissolved in DMSO. This was applied to the desired dispersion medium.
Conc	0.01%
Temperature	pH 7
Temperature	37 °C
Year	2007
Self assembly	Yes
Type of Self assembly	Firm hydrogel assembly
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Firm gel
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1006,
PMID	18070345
Peptide Name	Fmoc-Phe-Phe
Peptide sequence	FF
N-Terminal Modification	Fmoc
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	Confocal Microscopy
Solvent	Dispersion medium= MEM, DMSO (gelling agent)= 25mg/ml
Method	Lyophilized Fmoc-Phe-Phe dipeptide was weighed and dissolved in DMSO. This was applied to the desired dispersion medium.
Conc	0.005%
Temperature	pH 7
Temperature	37 °C
Year	2007
Self assembly	No
Type of Self assembly	Unstable hydrogel assembly
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Unstable
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1013,
PMID	12714741
Peptide Name	NH2-L-Phe-L-Phe-COOH
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	TEM (Transmission Electron Microscopy)
Solvent	Aqueous dispersion
Method	NH2-L-Phe-L-Phe-COOH dipeptide solublized at very high concentrations ( >=100 mg/ml) by dissolving the lyophilized peptide in 1,1,1,3,3,3 hexafluoro-2-propanol. The peptide appeared to be highly soluble in the organic solvent, a rapid assembly into ordered semicrystalline structures was observed visually within seconds after dilution into the aqueous solution at a final µM concentration range.
Conc	>=100 mg/ml stock soln
Temperature	80°C
Incubation Time	Within few minutes
Year	2003
Self assembly	Yes
Type of Self assembly	Nanotube
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	After 1 hour of incubation of the Phe-Phe peptide with proteinase K (0.02 mg/ml), no tubular structures were observed by electron microscopy examination (as compared with hundreds of tubular structures observed before the proteolysis).
	Nanotube
	150
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1014,
PMID	12714741
Peptide Name	NH2-D-Phe-D-Phe-COOH
Peptide sequence	ff
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	TEM (Transmission Electron Microscopy)
Solvent	Aqueous dispersion
Method	NH2-D-Phe-D-Phe-COOH dipeptide solublized at very high concentrations ( >=100 mg/ml) by dissolving the lyophilized peptide in 1,1,1,3,3,3 hexafluoro-2-propanol. The peptide appeared to be highly soluble in the organic solvent, a rapid assembly into ordered semicrystalline structures was observed visually within seconds after dilution into the aqueous solution at a final µM concentration range.
Conc	>=100 mg/ml stock soln
Temperature	80°C
Incubation Time	Within few minutes
Year	2003
Self assembly	Yes
Type of Self assembly	Nanotube
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	No notable variation could be observed before and after the incubation of the D-Phe-D-Phe peptide with the enzyme proteinase K (0.02 mg/ml).
	Nanotube
	150
	ff
	N[C@H](Cc1ccccc1)C(=O)N[C@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1015,
PMID	16430299
Peptide Name	Diphenylalanine peptide
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	SEM (Scanning Electron Microscopy), TEM (Transmission Electron Microscopy), CD (Circular Dichroism spectroscopy)
Solvent	Aqueous dispersion
Method	Lyophilized form of the peptides dissolved in 1,1,1,3,3,3-hexafluoro-2-propanol at a concentration of 100 mg/mL. Peptide stock solution was diluted in double distilled (dd) H2O to a final concentration of 2 mg/mL incubated in a water bath at 80 °C for 1 h.
Conc	2 mg/ml
Temperature	Stable upto 90°C
Incubation Time	Within few minutes
Year	2006
Self assembly	Yes
Type of Self assembly	Nanotube
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	In addition to thermal stability, the peptide nanotubes were chemically stable in organic solvents
	Nanotube
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1019,
PMID	16719470
Peptide Name	Diphenylalanine peptide
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	AFM (Atomic Force Microscopy)
Solvent	Aqueous dispersion
Method	Fresh stock solutions were prepared by dissolving the lyophilized peptides in 1,1,1,3,3,3-hexafluoro-2-propanol (Sigma Aldrich) at a concentration of 100 mg/mL. Peptide stock solution was diluted in double distilled (dd) H2O to a final concentration of 2 mg/mL. Samples were diluted in Elgar water to a final concentration of 0.2 or 1 mg/mL prior to dropping a 10 íL aliquot onto freshly cleaved mica and were subsequently dried in a vacuum generator.
Conc	1mg/ml
Temperature	Stable upto 100°C
Year	2006
Self assembly	Yes
Type of Self assembly	Nanotube
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	The nanotubes are stable at temperatures up to 100°C, but on heating to higher temperatures begin to lose their structural integrity with an apparent collapse in tubular structure.
	Nanotube
	525
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1020,
PMID	17328086
Peptide Name	Cationic dipeptide nanotubes (CDPNTs) (H-Phe-Phe-NH2·HCl)
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	HCl
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	AFM (Atomic Force Microscopy), TEM (Transmission Electron Microscopy)
Solvent	Aqueous dispersion
Method	The CDPNTs were selfassembled at physiological pH values
Conc	10 mg/ml
Temperature	pH 7.2
Temperature	Room temperature
Year	2007
Self assembly	Yes
Type of Self assembly	Nanotube
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Cationic dipeptides (H-Phe-Phe-NH2·HCl) self-assemble into nanotubes at physiological pH values and these cationic dipeptide nanotubes (CDPNTs) can also rearrange to form vesicles upon dilution.
	Nanotube
	190
	FF
	N.A.

Primary information
SAPdb ID	1021,
PMID	17328086
Peptide Name	Cationic dipeptide nanotubes (CDPNTs) (H-Phe-Phe-NH2·HCl)
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	HCl
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	AFM (Atomic Force Microscopy), TEM (Transmission Electron Microscopy)
Solvent	Aqueous dispersion
Method	The CDPNTs were selfassembled at physiological pH values
Conc	1 mg/ml
Temperature	pH 7.2
Temperature	Room temperature
Year	2007
Self assembly	Yes
Type of Self assembly	Vesicles
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Cationic dipeptides (H-Phe-Phe-NH2·HCl) self-assemble into nanotubes at physiological pH values and these cationic dipeptide nanotubes (CDPNTs) can also rearrange to form vesicles upon dilution.
	Nanovesicle
	100
	FF
	N.A.

Primary information
SAPdb ID	1022,
PMID	17328086
Peptide Name	Zwitterionic dipeptide diphenylalanine (l-Phe-l-Phe)
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	CD (Circular Dichroism spectroscopy)
Solvent	Aqueous dispersion
Method	Dipeptide could self-assemble into nanotubes at a concentration of 10 mg/mL
Conc	10 mg/ml
Temperature	pH 7.2
Temperature	Room temperature
Year	2007
Self assembly	Yes
Type of Self assembly	Nanotube
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable
	Nanotube
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1023,
PMID	18035858
Peptide Name	Diphenylalanine (H-Phe-Phe-OH)
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	SEM (Scanning Electron Microscopy)
Solvent	Aqueous dispersion
Method	Lyophilized form of the peptides dissolved in 1,1,1,3,3,3-HFP at a concentration of 50 or 100 mg/ml.
Conc	10 mg/ml
Year	2007
Self assembly	Yes
Type of Self assembly	Nanotube
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable
	Nanotube
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1024,
PMID	18035858
Peptide Name	Boc-Phe-Phe-OH
Peptide sequence	FF
N-Terminal Modification	Boc
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	SEM (Scanning Electron Microscopy)
Solvent	Aqueous dispersion
Method	Lyophilized form of the peptides dissolved in 1,1,1,3,3,3-HFP at a concentration of 50 or 100 mg/ml. For the preparation of nanospheres, a peptide stock solution was diluted in ethanol to a concentration of 10 mg/ml then immediately diluted in ddH2O to a final concentration of 5 mg/ml.
Conc	5 mg/ml
Year	2007
Self assembly	Yes
Type of Self assembly	Nanosphere
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Remarkable chemical and thermal stability and extraordinary mechanical strength. The averaged point stiffness of the nanotubes is 160 N/m, and they have a correspondingly high Young’s modulus of ∼19 Gpa.
	Nanosphere
	NA
	FF
	N.A.

Primary information
SAPdb ID	1025,
PMID	18035858
Peptide Name	Fmoc-Phe-Phe-OH
Peptide sequence	FF
N-Terminal Modification	Fmoc
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	SEM (Scanning Electron Microscopy)
Solvent	Aqueous dispersion
Method	Lyophilized form of the peptides dissolved in 1,1,1,3,3,3-HFP at a concentration of 50 or 100 mg/ml.
Conc	5 mg/ml
Year	2007
Self assembly	Yes
Type of Self assembly	Nanotube
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable
	Nanotube
	NA
	FF
	N.A.

Primary information
SAPdb ID	1026,
PMID	18035858
Peptide Name	Boc-Phe-Phe-OH
Peptide sequence	FF
N-Terminal Modification	Boc
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	SEM (Scanning Electron Microscopy)
Solvent	Aqueous dispersion
Method	Lyophilized form of the peptides dissolved in 1,1,1,3,3,3-HFP at a concentration of 50 or 100 mg/ml.For the preparation of nanotubes the 100 mg/ml peptide stock solutions in HFP was diluted into a final concentration of 2 mg/ml in ddH2O.
Conc	2 mg/ml
Year	2007
Self assembly	Yes
Type of Self assembly	Nanotube
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable
	Nanotube
	NA
	FF
	N.A.

Primary information
SAPdb ID	1194,
PMID	26295906
Peptide Name	Fmoc-FF
Peptide sequence	FF
N-Terminal Modification	Fmoc(fluorenylmethoxycarbonyl)
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	NMR diffusion - ordered spectroscopy (DOSY)
Solvent	Water+DMSO
Method	Peptide dissolved in deuterized water and DMSO solution at concentrations xH2O = 0.25–0.40. keep for sufficient time to ensure become gel.
Incubation Time	> 0.5 hours
Year	2015
Self assembly	Yes
Type of Self assembly	Solid Fibres
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanofibers
	NA
	FF
	N.A.

Primary information
SAPdb ID	1195,
PMID	26287262
Peptide Name	Boronic acid FF
Peptide sequence	FF
N-Terminal Modification	Carboxy-BA (Boronic acid)
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy), AFM (Atomic Force Microscopy)
Solvent	Water
Method	0.5-2 mg peptide was added to deionized water at 2 mg/mL. Concentrated NH4OH was then added in 0.5 μL aliquots to raise the pH to 10, yielding a homogenous solution. The pH was then lowered by conc. HCl or acetetic acid. When acidification was effected by diffusion of acetic acid vapor, a single, fibrous mass precipitated after several days upon reaching pH ≤ 5.
Conc	2mg/ml
Temperature	< or = 5
Year	2015
Self assembly	Yes
Type of Self assembly	Hydrogel ( consists of Nanoribbon)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	10
	FF
	N.A.

Primary information
SAPdb ID	1196,
PMID	26287262
Peptide Name	Boronic acid FF
Peptide sequence	FF
N-Terminal Modification	Carboxy-BA (Boronic acid)
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy), AFM (Atomic Force Microscopy)
Solvent	Water + 3M NaCl
Method	0.5-2 mg peptide was first dissolved in pH 7 phosphate buffer at 2 10 mg/mL. NaCl was then added in an amount corresponding to 1.5-3 M concentration and quickly vortexed to dissolve Shortly thereafter, a hazy suspension or a highly opaque, self-supporting hydrogel is formed.
Conc	2mg/ml
Temperature	> 5 or 7
Year	2015
Self assembly	Yes
Type of Self assembly	Hydrogel (consists of intertwined Fibril Network)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	10
	FF
	N.A.

Primary information
SAPdb ID	1197,
PMID	26018930
Peptide Name	Ferrocene-FF
Peptide sequence	FF
N-Terminal Modification	Ferrocene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	TEM (Transmission Electron Microscopy), SEM (Scanning Electron Microscopy)
Solvent	10% HFIP (1,1,1,3,3,3-hexafluoro-2-propanol) and 90% H2O (v/ v)
Method	Peptide powder was dissolved in 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) at a concentration of 4 mM. To yield a mixture of 10% HFIP and 90% H2O (v/ v) with 4 mM peptide conc. The turbid yellow suspension was incubated at 37 °C for 2 h without disturbance to form self assembled structure.
Conc	4mM
Temperature	< 5
Temperature	20°C
Incubation Time	2 hours
Year	2015
Self assembly	Yes
Type of Self assembly	Rectangular Nanotube
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanotube
	NA
	FF
	N.A.

Primary information
SAPdb ID	1198,
PMID	26018930
Peptide Name	Ferrocene-FF
Peptide sequence	FF
N-Terminal Modification	Ferrocene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	TEM (Transmission Electron Microscopy), SEM (Scanning Electron Microscopy)
Solvent	10% HFIP (1,1,1,3,3,3-hexafluoro-2-propanol) and 90% H2O (v/ v)
Method	Peptide powder was dissolved in 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) at a concentration of 20 mM. The Fc-FF HFIP solution (100 μL) was then injected into a 20 mM, pH 5.6 piperazine buffer solution (900 μL) to yield a mixture of 10% HFIP and 90% H2O (v/ v) with 4 mM. The turbid yellow suspension was incubated at 37 °C for 2 h without disturbance to form self assembled structure.
Conc	20mM
Temperature	5.6
Temperature	37°C
Incubation Time	2 hours
Year	2015
Self assembly	Yes
Type of Self assembly	Nanofiber
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanofibers
	NA
	FF
	N.A.

Primary information
SAPdb ID	1199,
PMID	26018930
Peptide Name	Ferrocene-FF
Peptide sequence	FF
N-Terminal Modification	Ferrocene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	TEM (Transmission Electron Microscopy), SEM (Scanning Electron Microscopy)
Solvent	10% HFIP (1,1,1,3,3,3-hexafluoro-2-propanol) and 90% Water (v/ v) + (R)-(-)-2-methylpiperazine
Method	Peptide powder was dissolved in 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) at a concentration of 20 mM. The Fc-FF HFIP solution (100 μL) was then injected into a 20 mM, pH 5.6 piperazine buffer solution (900 μL) to yield a mixture of 10% HFIP and 90% H2O (v/ v) with 4 mM. The turbid yellow suspension was incubated at 37 °C for 2 h without disturbance to form self assembled structure.
Conc	4mM
Temperature	5.6
Temperature	37°C
Incubation Time	2 hours
Year	2015
Self assembly	Yes
Type of Self assembly	Nanohelicals (right handed)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanohelicals
	100000
	FF
	N.A.

Primary information
SAPdb ID	1200,
PMID	26018930
Peptide Name	Ferrocene-FF
Peptide sequence	FF
N-Terminal Modification	Ferrocene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	TEM (Transmission Electron Microscopy), SEM (Scanning Electron Microscopy)
Solvent	10% HFIP (1,1,1,3,3,3-hexafluoro-2-propanol) and 90% Water (v/ v) + (S)-(+)-2-methylpiperazine
Method	Peptide powder was dissolved in 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) at a concentration of 20 mM. The Fc-FF HFIP solution (100 μL) was then injected into a 20 mM, pH 5.6 piperazine buffer solution (900 μL) to yield a mixture of 10% HFIP and 90% H2O (v/ v) with 4 mM. This suspension was incubated at 37 °C for 2 h without disturbance to form self assembled structure.
Conc	4mM
Temperature	5.6
Temperature	37°C
Incubation Time	2 hours
Year	2015
Self assembly	Yes
Type of Self assembly	Nanofibers (right handed)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanohelicals
	100000
	FF
	N.A.

Primary information
SAPdb ID	1201,
PMID	26018930
Peptide Name	Ferrocene-FF
Peptide sequence	FF
N-Terminal Modification	Ferrocene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	TEM (Transmission Electron Microscopy), SEM (Scanning Electron Microscopy)
Solvent	10% HFIP + 90% piperazine buffer solution (20 mM, pH 5.6)
Method	Peptide powder was dissolved in 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) at a concentration of 20 mM. The Fc-FF HFIP solution (100 μL) was then injected into a 20 mM, pH 5.6 piperazine buffer solution (900 μL) to yield a mixture of 10% HFIP and 90% H2O (v/ v) with 4 mM. This suspension was incubated at 37 °C for 2 h without disturbance to form self assembled structure.
Conc	4mM
Temperature	5.3 - 5.6
Temperature	37°C
Incubation Time	2 hours
Year	2015
Self assembly	Yes
Type of Self assembly	Highly twisted chiral Nanostructures (big twists)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanohelicals
	NA
	FF
	N.A.

Primary information
SAPdb ID	1202,
PMID	26018930
Peptide Name	Ferrocene-FF
Peptide sequence	FF
N-Terminal Modification	Ferrocene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	TEM (Transmission Electron Microscopy), SEM (Scanning Electron Microscopy)
Solvent	10% HFIP + 90% piperazine buffer solution (20 mM, pH 5.6)
Method	Peptide powder was dissolved in 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) at a concentration of 20 mM. The Fc-FF HFIP solution (100 μL) was then injected into a 20 mM, pH 6 piperazine buffer solution (900 μL) to yield a mixture of 10% HFIP and 90% H2O (v/ v) with 4 mM. This suspension was incubated at 37 °C for 2 h without disturbance to form self assembled structure.
Conc	4mM
Temperature	> 6
Temperature	37°C
Incubation Time	2 hours
Year	2015
Self assembly	Yes
Type of Self assembly	Heterogenous chiral Nanostructures (Nanohelix)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable for 24 hours
	Nanohelicals
	NA
	FF
	N.A.

Primary information
SAPdb ID	1203,
PMID	26018930
Peptide Name	Ferrocene-FF
Peptide sequence	FF
N-Terminal Modification	Ferrocene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	TEM (Transmission Electron Microscopy), SEM (Scanning Electron Microscopy)
Solvent	Ethylenediamine + 10% HFIP (1,1,1,3,3,3-hexafluoro-2-propanol) and 90% H2O (v/ v)
Method	Peptide powder was dissolved in 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) at a concentration of 20 mM. The Fc-FF HFIP solution (100 μL) was then injected into a 20 mM, pH 5.6 ethylenediamine solution (900 μL) to yield a mixture of 10% HFIP and 90% H2O (v/ v) with 4 mM. This suspension was incubated at 37 °C for 2 h without disturbance to form self assembled structure.
Conc	4mM
Temperature	5.6
Temperature	37°C
Incubation Time	2 hours
Year	2015
Self assembly	Yes
Type of Self assembly	Right Handed Chiral Nanostructure
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanohelicals
	150
	FF
	N.A.

Primary information
SAPdb ID	1204,
PMID	26018930
Peptide Name	Ferrocene-FF
Peptide sequence	FF
N-Terminal Modification	Ferrocene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	TEM (Transmission Electron Microscopy), SEM (Scanning Electron Microscopy)
Solvent	1, 4- diaminobutane + 10% HFIP (1,1,1,3,3,3-hexafluoro-2-propanol) and 90% H2O (v/ v)
Method	Peptide powder was dissolved in 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) at a concentration of 20 mM. The Fc-FF HFIP solution (100 μL) was then injected into a1, 4- diaminobutane to yield a mixture of 10% HFIP and 90% H2O (v/ v) with 4 mM. This suspension was incubated at 37 °C for 2 h without disturbance to form self assembled structure.
Conc	4mM
Temperature	5.6
Temperature	37°C
Incubation Time	2 hours
Year	2015
Self assembly	Yes
Type of Self assembly	Amorphous aggregate
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	None
	NA
	FF
	N.A.

Primary information
SAPdb ID	1205,
PMID	26018930
Peptide Name	Ferrocene-FF
Peptide sequence	FF
N-Terminal Modification	Ferrocene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	TEM (Transmission Electron Microscopy), SEM (Scanning Electron Microscopy)
Solvent	Na+ and K+
Method	Peptide powder was dissolved in 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) at a concentration of 20 mM. The Fc-FF HFIP solution (100 μL) in presence of NA+, or K+ ions yield a mixture of 10% HFIP and 90% H2O (v/ v) with 4 mM. This suspension was incubated at 37 °C for 2 h without disturbance to form self assembled structure.
Conc	4mM
Temperature	5.6
Temperature	37°C
Incubation Time	2 hours
Year	2015
Self assembly	Yes
Type of Self assembly	Rectangular microtube
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Others
	1000
	FF
	N.A.

Primary information
SAPdb ID	1206,
PMID	26018930
Peptide Name	Ferrocene-FF
Peptide sequence	FF
N-Terminal Modification	Ferrocene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	TEM (Transmission Electron Microscopy), SEM (Scanning Electron Microscopy)
Solvent	10% HFIP (1,1,1,3,3,3-hexafluoro-2-propanol) and 90% H2O (v/ v)
Method	Peptide powder was dissolved in 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) at a concentration of 4 mM. To yield a mixture of 10% HFIP and 90% H2O (v/ v) with 4 mM peptide conc. The turbid yellow suspension was incubated at 37 °C for 2 h without disturbance to form self assembled structure.
Conc	4mM
Temperature	5.6
Temperature	< 30°C
Incubation Time	2 hours
Year	2015
Self assembly	Yes
Type of Self assembly	Thick microbelt
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Others
	NA
	FF
	N.A.

Primary information
SAPdb ID	1207,
PMID	26018930
Peptide Name	Ferrocene-FF
Peptide sequence	FF
N-Terminal Modification	Ferrocene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	TEM (Transmission Electron Microscopy), SEM (Scanning Electron Microscopy)
Solvent	10% HFIP (1,1,1,3,3,3-hexafluoro-2-propanol) and 90% H2O (v/ v)
Method	Peptide powder was dissolved in 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) at a concentration of 4 mM. To yield a mixture of 10% HFIP and 90% H2O (v/ v) with 4 mM peptide conc. The turbid yellow suspension was incubated at 37 °C for 2 h without disturbance to form self assembled structure.
Conc	4mM
Temperature	5.6
Temperature	> 37°C
Incubation Time	2 hours
Year	2015
Self assembly	Yes
Type of Self assembly	Big twist
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable at temperature > 37°C for 48 hours; Unstable at < 37°C
	Nanoribbon
	NA
	FF
	N.A.

Primary information
SAPdb ID	1208,
PMID	26018930
Peptide Name	Ferrocene-FF
Peptide sequence	FF
N-Terminal Modification	Ferrocene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	TEM (Transmission Electron Microscopy), SEM (Scanning Electron Microscopy)
Solvent	10% 2-propanol/ 90% H2O
Method	Peptide powder was dissolved in 2-propanol) at a concentration of 4 mM. To yield a mixture of 10% 2-propanol and 90% H2O (v/ v) with 4 mM peptide conc. The suspension was incubated at 37 °C for 2 h without disturbance to form self assembled structure.
Conc	4mM
Temperature	5.6
Temperature	37°C
Incubation Time	2 hours
Year	2015
Self assembly	Yes
Type of Self assembly	Nanoribbon(twist)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanoribbon
	100
	FF
	N.A.

Primary information
SAPdb ID	1209,
PMID	26018930
Peptide Name	Ferrocene-FF
Peptide sequence	FF
N-Terminal Modification	Ferrocene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	TEM (Transmission Electron Microscopy), SEM (Scanning Electron Microscopy)
Solvent	10% acetonitrile + 90% H2O,
Method	Peptide powder was dissolved in acetonitrile at a concentration of 4 mM. To yield a mixture of 10% HFIP and 90% H2O (v/ v) with 4 mM peptide conc. The turbid yellow suspension was incubated at 37 °C for 2 h without disturbance to form self assembled structure.
Conc	4mM
Temperature	5.6
Temperature	37°C
Incubation Time	2 hours
Year	2015
Self assembly	Yes
Type of Self assembly	Nanoribbon(twist)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanoribbon
	200
	FF
	N.A.

Primary information
SAPdb ID	1210,
PMID	26018930
Peptide Name	Ferrocene-FF
Peptide sequence	FF
N-Terminal Modification	Ferrocene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	TEM (Transmission Electron Microscopy), SEM (Scanning Electron Microscopy)
Solvent	10% acetonitrile and 90% H2O (20 mM piperazine)
Method	Peptide powder was dissolved in acetonitrile at a concentration of 20 mM. this solution was then injected into a 20 mM, pH 5.6 piperazine buffer solution (900 μL) to yield a mixture of 10% acetonitrile and 90% H2O (v/ v) with 4 mM. The suspension was incubated at 37 °C for 2 h without disturbance to form self assembled structure.
Conc	4 mM
Temperature	5.6
Temperature	50°C
Incubation Time	2 hours
Year	2015
Self assembly	Yes
Type of Self assembly	Nanoscrew
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Others
	NA
	FF
	N.A.

Primary information
SAPdb ID	1211,
PMID	26018930
Peptide Name	Ferrocene-FF
Peptide sequence	FF
N-Terminal Modification	Ferrocene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	TEM (Transmission Electron Microscopy), SEM (Scanning Electron Microscopy)
Solvent	10% 2-propanol and 90% PBS solution (100 mM)
Method	Peptide powder was dissolved in 2-propanol at a concentration of 4 mM. To yield a mixture of 10% 2-propanol and 90% PBS (v/ v) with 4 mM peptide conc. This suspension was incubated at 37 °C for 2 h without disturbance to form self assembled structure.
Conc	4 mM
Temperature	5.6
Temperature	37°C
Incubation Time	2 hours
Year	2015
Self assembly	Yes
Type of Self assembly	Nanotube
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanotube
	NA
	FF
	N.A.

Primary information
SAPdb ID	1214,
PMID	25775220
Peptide Name	2-Thiopene diphenyl alanine
Peptide sequence	FF
N-Terminal Modification	2-thiopene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy)
Solvent	Water + Sodium hydroxide
Method	The gelator was added to 2 mL of water with an equimolar amount of sodium hydroxide (0.1 M, aqueous). For solutions prepared with potassium carbonate and potassium hydroxide again an equimolar amount of 0.1 M solutions were used. The solution was stirred until all the gelator was dissolved. This solution was then transferred to a vial containing a 2.5 mg/mL of glucono-δ-lactone (GdL) and shaken gently. This was then left to stand to allow gelation to occur within a few hours.
Conc	2.5 mg/mL
Temperature	11
Temperature	Room temperature
Incubation Time	16 hours
Year	2012
Self assembly	Yes
Type of Self assembly	Transparent gel (containing Nanofibres)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1215,
PMID	25775220
Peptide Name	2-Thiopene diphenyl alanine
Peptide sequence	FF
N-Terminal Modification	2-thiopene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy)
Solvent	Water + Sodium hydroxide
Method	The gelator was added to 2 mL of water with an equimolar amount of sodium hydroxide (0.1 M, aqueous). For solutions prepared with potassium carbonate and potassium hydroxide again an equimolar amount of 0.1 M solutions were used. The solution was stirred until all the gelator was dissolved. This solution was then transferred to a vial containing a 2.5 mg/mL of glucono-δ-lactone (GdL) and shaken gently. This was then left to stand to allow gelation to occur within a few hours.
Conc	2.5 mg/mL
Temperature	11
Temperature	Room temperature
Incubation Time	72 hours
Year	2012
Self assembly	Yes
Type of Self assembly	Turbid gel (containing Nanospheres)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	1000
	FF
	N.A.

Primary information
SAPdb ID	1216,
PMID	24482003
Peptide Name	Peptide-porphyrin
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy), AFM (Atomic Force Microscopy) and TEM (Transmission Electron Microscopy)
Solvent	Water+Sulfonated porphyrin
Method	2 mg FF was first dissolved in a 20 μL aqueous solution of HCl (1 M), followed by dilution with an 1mM aqueous solution of anionic tetrakis(4-sulfonatophenyl)porphine ([H2TPPS]). Final concentrations of [H2TPPS] and FF were 0.1 mM and 6.4 mM, respectively and pH was 1.9. Mixing the solutions gave a green turbid suspension that was aged for 2 days. Microspheres were separated and collected from the aqueous suspension by centrifugation
Conc	6.4mM
Temperature	1.9
Temperature	Room temperature
Incubation Time	48 hours
Year	2014
Self assembly	Yes
Type of Self assembly	Microsphere
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable against photodegradation
	Others
	4000
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1217,
PMID	25621167
Peptide Name	Diphenylalanine
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	FE - SEM (Field Emission Scanning Electron Microscopy or FE - SEM)
Solvent	Water
Method	Fresh stock solutions of Phe were prepared by dissolving Phe in distilled water at concentrations of 10, 25, 50, 100, and 150 mM. Fibril structure formed by following two techniques: (1)Conventional drop-casting: 3 mL of Phe–Phe solution was dropped on a clean stainless steel substrate and allowed to dry at 25°C in a vacuum for 12 h prior to subsequent characterization; (2) Directional freeze-drying: 1.5 mL of Phe–Phe solution was pipetted into a 2 mL centrifuge tube. The tube was placed into liquid nitrogen or a 20°C or 80°C freezer
Conc	2mM
Temperature	7
Temperature	(-)20°C
Year	2015
Self assembly	Yes
Type of Self assembly	Nanofiber
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanofibers
	10000
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1229,
PMID	25354784
Peptide Name	Compound 1
Peptide sequence	FF
N-Terminal Modification	Indole acetic acid
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	TEM (Transmission Electron Microscopy), AFM (Atomic Force Microscopy)
Solvent	1mM Phosphate buffer saline
Method	Compound 1 dissolved in 1mM PBS(phosphate buffer saline) ,the solution is heated to 90°C and allowed to cool, forming a transparent gel that gradually changes to an opaque gel over time.
Conc	1% w/v
Temperature	Heated at 90°C and followed by cooling
Incubation Time	30 minutes - 12hours
Year	2014
Self assembly	Yes
Type of Self assembly	Hydrogel (Containing Nanofibres)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable hydogel but degraded in conc. NaCl solution
	Hydrogel
	250
	FF
	N.A.

Primary information
SAPdb ID	1230,
PMID	25354784
Peptide Name	Compound 1
Peptide sequence	FF
N-Terminal Modification	Indole acetic acid
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	TEM (Transmission Electron Microscopy), AFM (Atomic Force Microscopy)
Solvent	DMSO + water
Method	Compound 1 dissolved in DMSO and diluted with water, in the soultion GdL (gluco-delta-lactone) is added to maintain the pH. Solution gelate with 30 minutes to 24 hours.
Conc	> 0.4% w/v
Incubation Time	5 -10 minutes
Year	2014
Self assembly	Yes
Type of Self assembly	Transparent Gel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable hydogel but degraded in conc. NaCl solution
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1231,
PMID	25259412
Peptide Name	FF
Peptide sequence	FF
N-Terminal Modification	Conjugate with TTF
C-Terminal Modification	Amidation
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Conjugate
Conjugate partner	Tetrathiafulvalene (TTF)
Technique	TEM (Transmission Electron Microscopy), AFM (Atomic Force Microscopy), UV - vis - NIR, FTIR and CD (Circular Dichroism spectroscopy)
Solvent	Chloroform
Method	The TTF-FF-NH2 gelator (11.7 mg, 20mM) was mixed in a 1ml solvent. The mixture was vortexed followed by sonication for few seconds and heated to dissolve. The sample was cooled to room temperature and left for few hours to gelation.
Conc	20mM
Temperature	Room temperature
Incubation Time	30 minutes
Year	2014
Self assembly	Yes
Type of Self assembly	Organogel (consists of Nanofibers)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	Magnetically induced
	Stable for months under ambient conditions
	Organogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1232,
PMID	25259412
Peptide Name	FF
Peptide sequence	FF
N-Terminal Modification	Conjugate with TTF
C-Terminal Modification	Amidation
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Conjugate
Conjugate partner	Tetrathiafulvalene (TTF)
Technique	TEM (Transmission Electron Microscopy), AFM (Atomic Force Microscopy), UV - vis - NIR, FTIR and CD (Circular Dichroism spectroscopy)
Solvent	Ethylacetate
Method	The TTF-FF-NH2 gelator (11.7 mg, 20mM) was mixed in a 1ml solvent. The mixture was vortexed followed by sonication for few seconds and heated to dissolve. The sample was cooled to room temperature and left for few hours to gelation.
Conc	20mM
Temperature	Room temperature
Incubation Time	12 hours
Year	2014
Self assembly	Yes
Type of Self assembly	Organogel (consists of Nanofibers)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	Magnetically induced
	Stable for months under ambient conditions
	Organogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1233,
PMID	25198430
Peptide Name	FF
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy)
Solvent	Methanol + HFIP (1,1,1,3,3,3-hexafluoro-2-propanol)
Method	Diphenylalanine (FF) first dissolved in 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) at a concentration of 100 mg/mL. The corresponding stock solution was then diluted to a final concentration of 1 mg/mL in methanol.
Conc	1mg/ml
Temperature	~64.7°C
Incubation Time	3 - 20 minutes
Year	2014
Self assembly	Yes
Type of Self assembly	Microsphere with microtube
Tertiary Structure (Technique)	Not Predicted),
	Linear
	Artificial supersaturation caused by Joule heating effect using voltage 100V
	NA
	Others
	7500
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1235,
PMID	25068387
Peptide Name	NapFF
Peptide sequence	FF
N-Terminal Modification	Napthalene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Conjugate
Conjugate partner	Napthalene
Technique	TEM (Transmission Electron Microscopy), Cryo - SEM (Scanning Electron Microscopy)
Solvent	Deionized water + 1M Sodium hydroxide + 0.5M HCl
Method	Peptide was initially suspended in 200 μL in Water. 1M NaOH added to dissolve the peptide and to lower the pH to 6-7 using HCl (0.5M) added. Homogenous gel formed after keeping it for 24 hours
Conc	> 0.5 w%
Temperature	pH 6 -7
Incubation Time	24 hours
Year	2014
Self assembly	Yes
Type of Self assembly	Hydrogel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1241,
PMID	20695592
Peptide Name	Dipeptide 7
Peptide sequence	FF
N-Terminal Modification	Napthalene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Conjugate
Conjugate partner	Bromo-Napthalene
Technique	TEM (Transmission Electron Microscopy)
Solvent	Deionized water + 0.1 M Sodium hydroxide + glucono-δ-lactone (GdL)
Method	Stock solutions of dipeptide-conjugates at a concentration of (0.5 wt%) were prepared and equimolar NaOH (0.1M ) added to it. These were then diluted with pH 10 water to a number of concentrations. To adjust the pH, for each dipeptide-conjugate solution and required quantity of GdL is added to solution to ensure final pH between 3.2 -3.6. Samples were left to stand at least 24 h.
Conc	0.5 wt%
Temperature	3.4 +/- 0.2.
Temperature	Room temperature
Incubation Time	24 hours
Year	2010
Self assembly	Yes
Type of Self assembly	Transparent Gel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1247,
PMID	20695592
Peptide Name	Dipeptide 13
Peptide sequence	FF
N-Terminal Modification	Bromo-Napthalene or napthalene derivative
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Conjugate
Conjugate partner	Nitrile-Napthalene
Technique	TEM (Transmission Electron Microscopy)
Solvent	Deionized water + 0.1 M Sodium hydroxide + glucono-δ-lactone (GdL)
Method	Stock solutions of dipeptide-conjugates at a concentration of (0.5 wt%) were prepared and equimolar NaOH (0.1M ) added to it. These were then diluted with pH 10 water to a number of concentrations. To adjust the pH, for each dipeptide-conjugate solution and required quantity of GdL is added to solution to ensure final pH between 3.2 -3.6. Samples were left to stand at least 24 h.
Conc	0.5 wt%
Temperature	3.4 +/- 0.2.
Temperature	Room temperature
Incubation Time	24 hours
Year	2010
Self assembly	Yes
Type of Self assembly	Turbid Gel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Others
	NA
	FF
	N.A.

Primary information
SAPdb ID	1253,
PMID	22468743
Peptide Name	Diphenylalanine
Peptide sequence	FF
N-Terminal Modification	Cyano-Napthalene or napthalene derivative
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	Insilico tools i.e, Coarse - grained molecular dynamics (MD) simulations and GROMACS software
Solvent	Water
Method	40 MD simulations performed on a system consisting of 600 FF peptides at peptide concentrations: 155mg/mL
Conc	155 mg/ml
Temperature	37°C
Incubation Time	60 - 1200 nanoseconds
Year	2012
Self assembly	Yes
Type of Self assembly	Flat bilayer with holes shape ( in 9/10 MD runs); Nanotube (in 1/10 MD runs)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanotube
	5.35
	FF
	N.A.

Primary information
SAPdb ID	1254,
PMID	22468743
Peptide Name	Diphenylalanine
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	Insilico tools i.e, Coarse - grained molecular dynamics (MD) simulations and GROMACS software
Solvent	Water
Method	40 MD simulations performed on a system consisting of 600 FF peptides at peptide concentrations: 85mg/mL
Conc	85 mg/ml
Temperature	37°C
Incubation Time	60 - 1200 nanoseconds
Year	2012
Self assembly	Yes
Type of Self assembly	Spherical vesicle ( in 7/10 MD runs); Nanotube (in 2/10 MD runs); Bialyer shape (in 1/10 MD runs)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable
	Nanovesicle, Nanotube
	9.2
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1255,
PMID	22468743
Peptide Name	Diphenylalanine
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	Insilico tools i.e, Coarse - grained molecular dynamics (MD) simulations and GROMACS software
Solvent	Water
Method	40 MD simulations performed on a system consisting of 600 FF peptides at peptide concentrations: 120mg/mL
Conc	120 mg/ml
Temperature	37°C
Incubation Time	60 - 1200 nanoseconds
Year	2012
Self assembly	Yes
Type of Self assembly	vesicle (in 3/10 MD runs); Nanotube ( in 3/10 MD runs); Flat bialyer with holes shape (in 4/10 MD runs)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanovesicle, Nanotube
	9.2
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1259,
PMID	19496552
Peptide Name	Diphenylalanine
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	AFM (Atomic Force Microscopy
Solvent	1,1,1,3,3,3-hexafluoro-2-propanol (HFIP)/water
Method	Peptide was dissolved in HFIP (1,1,1,3,3,3-hexafluoro-2-propanol) at 100mg/ml conc., solution is further diluted with water at pH 6 to make final concenteration 2mg/ml. Peptide solutions were placed onto freshly cleaved mica substrates and and dried under nitrogen gas.
Conc	2mg/ml
Temperature	6
Temperature	Room temperature
Year	2009
Self assembly	Yes
Type of Self assembly	Nanotube
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable at 120°C
	Nanotube
	175
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1269,
PMID	19705843
Peptide Name	Fmoc-FF
Peptide sequence	FF
N-Terminal Modification	Fmoc(fluorenylmethoxycarbonyl)
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	TEM (Transmission Electron Microscopy), AFM (Atomic Force Microscopy)
Solvent	Water
Method	Peptide first dissolved in DMSO and then diluted in water to their final concentration 5mg/ml. Self assembled structure formed at room temperature
Conc	5mg/ml
Temperature	pH 3 - 12
Temperature	Room temperature
Year	2009
Self assembly	Yes
Type of Self assembly	Hydrogel (Tangled Fibrous Nano structure)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable at pH 3 - 12
	Hydrogel
	20
	FF
	N.A.

Primary information
SAPdb ID	1274,
PMID	20000323
Peptide Name	Diphenylalanine
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy), AFM (Atomic Force Microscopy)
Solvent	Water
Method	Dipeptide was dissolved in solvent, at a concentration of 2 mg/mL at 70°C for 10 min and cooled to room temperature. Each peptide solution (50 μL) was then placed onto cleaned silicon wafers or glass slides and dried until the solvent evaporated and self assembled structure formed.
Conc	2mg/ml
Temperature	25°C
Year	2009
Self assembly	Yes
Type of Self assembly	Tubular Nanostructure
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable in proteinase solution
	Nanotube
	1650
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1275,
PMID	20000323
Peptide Name	Diphenylalanine
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy), AFM (Atomic Force Microscopy)
Solvent	Methanol
Method	Dipeptide was dissolved in solvent, at a concentration of 2 mg/mL at 70°C for 10 min and cooled to room temperature. Each peptide solution (50 μL) was then placed onto cleaned silicon wafers or glass slides and dried until the solvent evaporated and self assembled structure formed.
Conc	2mg/ml
Temperature	25°C
Year	2009
Self assembly	Yes
Type of Self assembly	Tubular Nanostructure
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable in proteinase solution
	Nanotube
	1650
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1276,
PMID	20000323
Peptide Name	Diphenylalanine
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy), AFM (Atomic Force Microscopy)
Solvent	Ethanol
Method	Dipeptide was dissolved in solvent, at a concentration of 2 mg/mL at 70°C for 10 min and cooled to room temperature. Each peptide solution (50 μL) was then placed onto cleaned silicon wafers or glass slides and dried until the solvent evaporated at 80°C and self assembled structure formed.
Conc	2mg/ml
Temperature	80°C
Year	2009
Self assembly	Yes
Type of Self assembly	Tubular Nanostructure
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable in proteinase solution
	Nanotube
	1650
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1277,
PMID	20000323
Peptide Name	Diphenylalanine
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy), AFM (Atomic Force Microscopy)
Solvent	Acetone
Method	Dipeptide was dissolved in solvent, at a concentration of 2 mg/mL at 70°C for 10 min and cooled to room temperature. Each peptide solution (50 μL) was then placed onto cleaned silicon wafers or glass slides and dried until the solvent evaporated at 80° and self assembled structure formed.
Conc	2mg/ml
Temperature	80°C
Year	2009
Self assembly	Yes
Type of Self assembly	Nanovesicle
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable in proteinase solution
	Nanovesicle
	1100
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1278,
PMID	20000323
Peptide Name	Diphenylalanine
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy), AFM (Atomic Force Microscopy)
Solvent	Tetrahydrofuran (THF)
Method	Dipeptide was dissolved in solvent, at a concentration of 2 mg/mL at 70°C for 10 min and cooled to room temperature. Each peptide solution (50 μL) was then placed onto cleaned silicon wafers or glass slides and dried until the solvent evaporated and self assembled structure formed.
Conc	2mg/ml
Temperature	25°C
Year	2009
Self assembly	No
Type of Self assembly	No self assembled structure
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	None
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1279,
PMID	20000323
Peptide Name	Diphenylalanine
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy), AFM (Atomic Force Microscopy)
Solvent	Chloroform
Method	Dipeptide was dissolved in solvent, at a concentration of 2 mg/mL at 70°C for 10 min and cooled to room temperature. Each peptide solution (50 μL) was then placed onto cleaned silicon wafers or glass slides and dried until the solvent evaporated and self assembled structure formed.
Conc	2mg/ml
Temperature	25°C
Year	2009
Self assembly	No
Type of Self assembly	No self assembled structure
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	None
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1280,
PMID	20000323
Peptide Name	Diphenylalanine
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy), AFM (Atomic Force Microscopy)
Solvent	Toluene
Method	Dipeptide was dissolved in solvent, at a concentration of 2 mg/mL at 70°C for 10 min and cooled to room temperature. Each peptide solution (50 μL) was then placed onto cleaned silicon wafers or glass slides and dried until the solvent evaporated and self assembled structure formed.
Conc	2mg/ml
Temperature	25°C
Year	2009
Self assembly	No
Type of Self assembly	No self assembled structure
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	None
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1281,
PMID	20000323
Peptide Name	Diphenylalanine
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy), AFM (Atomic Force Microscopy)
Solvent	Benzene
Method	Dipeptide was dissolved in solvent, at a concentration of 2 mg/mL at 70 °C for 10 min and cooled to room temperature. Each peptide solution (50 μL) was then placed onto cleaned silicon wafers or glass slides and dried until the solvent evaporated and self assembled structure formed.
Conc	2mg/ml
Temperature	25°C
Year	2009
Self assembly	No
Type of Self assembly	No self assembled structure
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	None
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1284,
PMID	22890605
Peptide Name	CNNapFF
Peptide sequence	FF
N-Terminal Modification	CN-napthol
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Conjugate
Conjugate partner	CN-napthol
Technique	SEM (Scanning Electron Microscopy)
Solvent	Sodium hydoxide(0.1 M )
Method	A 0.5 wt% stock solution of dipeptide at pH 9 – 10 prepaed by adding 1 equivalent of sodium hydroxide solution 0.1 M solution) with stirring atleast for 1 hour to dissolve, PAG (1 molar equivalent) was added to this solution before leaving to stir overnight and it lowers the pH of solution to 6. To form gels, 2 mL of stock solution was placed in a 7 mL Sterilin cup for 14 hours and UV light was irradiated from a 40 W Spectroline X-series UV lamp (wavelength 254 nm) .
Conc	5mg/ml
Temperature	6
Temperature	Room temperature
Incubation Time	14 hours
Year	2012
Self assembly	Yes
Type of Self assembly	Turbid gel (Nanofibers)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	70
	FF
	N.A.

Primary information
SAPdb ID	1285,
PMID	22890605
Peptide Name	7MeOFF
Peptide sequence	FF
N-Terminal Modification	7-methoxt-2-napthol
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Conjugate
Conjugate partner	7-methoxt-2-napthol
Technique	SEM (Scanning Electron Microscopy)
Solvent	Sodium hydoxide(0.1 M )
Method	A 0.5 wt% stock solution of dipeptide at pH 9 – 10 prepaed by adding 1 equivalent of sodium hydroxide solution 0.1 M solution) with stirring atleast for overnight to dissolve, PAG (1 molar equivalent) was added to this solution before leaving to stir overnight and it lowers the pH of solution to 6.3. To form gels, 2 mL of stock solution was placed in a 7 mL Sterilin cup for 14 hours and UV light was irradiated from a 40 W Spectroline X-series UV lamp (wavelength 254 nm) .
Conc	5mg/ml
Temperature	6.3
Temperature	Room temperature
Incubation Time	14 hours
Year	2012
Self assembly	Yes
Type of Self assembly	Turbid gel (Nanofibers)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	10
	FF
	N.A.

Primary information
SAPdb ID	1288,
PMID	22890605
Peptide Name	2NapFF
Peptide sequence	FF
N-Terminal Modification	Napthalene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Conjugate
Conjugate partner	Napthalene
Technique	SEM (Scanning Electron Microscopy)
Solvent	Sodium hydoxide(0.1 M )
Method	A 0.5 wt% stock solution of dipeptide at pH 9 – 10 prepaed by adding 1 equivalent of sodium hydroxide solution 0.1 M solution) with stirring atleast for 1 hour to dissolve, PAG (1 molar equivalent) was added to this solution before leaving to stir overnight and it lower the pH of solution to 6.4. To form gels, 2 mL of stock solution was placed in a 7 mL Sterilin cup for 14 hours and UV light was irradiated from a 40 W Spectroline X-series UV lamp (wavelength 254 nm) .
Conc	5mg/ml
Temperature	6.4
Temperature	Room temperature
Incubation Time	14 hours
Year	2012
Self assembly	No
Type of Self assembly	No gel formation
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	None
	NA
	FF
	N.A.

Primary information
SAPdb ID	1289,
PMID	22897679
Peptide Name	(polyA-FF-ME) or Poly(N-acryloyl-L-phenylalanyl-L-phenylalanine methyl ester)
Peptide sequence	FF
N-Terminal Modification	Acryloyl
C-Terminal Modification	Methyl esterification
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Mixture
Conjugate partner	PVP (Polyvinylpyrrolidone) and BP (benzoyl peroxide)
Technique	HR - SEM (High Resolution Scanning Electron Microscopy)
Solvent	Methoxy-ethanol
Method	30 mg of the vinylic monomer A-FF-ME, 10 mg PVP, and 2 mg of BP were added to 1 mL of nitrogen-bubbled 2-methoxy ethanol.The mixture was shaken at room temperature to dissolve the solids at conc 3% 1%, and 0.2% (w/v) AA-FF-ME, PVP, and BP, respectively. The mixture was then shaken at 75 οC for 18 h. The formed soluble polyA-FF-ME wasprecipitated as uniform nanoparticles by adding 100 μL of its solution to 1 mL distilled water.
Conc	3% w/v
Temperature	75°C
Incubation Time	18 hours
Year	2012
Self assembly	Yes
Type of Self assembly	Nanoparticle
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable for more than 233 h of heating
	Nanoparticle
	57
	FF
	N.A.

Primary information
SAPdb ID	1301,
PMID	23061818
Peptide Name	Boc-Phe-Phe-OH and NH2-Phe-Phe-OH
Peptide sequence	FF
N-Terminal Modification	Boc (t-butoxycarbonyl) on 1st dipeptide
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Mixture
Conjugate partner	Boc-Phe-Phe-OH + NH2-Phe-Phe-OH
Technique	SEM (Scanning Electron Microscopy), HR - SEM (High Resolution Scanning Electron Microscopy), TEM (Transmission Electron Microscopy), AFM (Atomic force Microscopy)
Solvent	HFP (1,1,1,3,3,3-hexafluoro-2-propanol) + 50% ethanol + 16 mMNaCl
Method	To coassemble the two peptides, we dissolved each peptide in 1,1,1,3,3,3-hexafluoro-2-propanol (HFP) and diluted them in 50% ethanol. The polarized solvent allowed the selfassembly of peptides.
Conc	5mg/ml (1st dipeptide) + 2mg/ml )2nd dipeptide
Temperature	~ 4.5
Temperature	Room temperature
Incubation Time	10 -24 hours
Year	2012
Self assembly	Yes
Type of Self assembly	Spherical structures with branching fibers
Tertiary Structure (Technique)	Not Predicted),
	Linear
	Co-assembly of two dipeptides
	Stable upto at 70°C
	Others
	800
	FF
	N.A.

Primary information
SAPdb ID	1302,
PMID	23061818
Peptide Name	Boc-Phe-Phe-OH and NH2-Phe-Phe-OH
Peptide sequence	FF
N-Terminal Modification	Boc (t-butoxycarbonyl) on 1st dipeptide
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Mixture
Conjugate partner	Boc-Phe-Phe-OH + NH2-Phe-Phe-OH
Technique	SEM (Scanning Electron Microscopy), HR - SEM (High Resolution Scanning Electron Microscopy), TEM (Transmission Electron Microscopy), AFM (Atomic force Microscopy)
Solvent	HFP (1,1,1,3,3,3-hexafluoro-2-propanol) + 50% ethanol + 16 mMNaCl
Method	To coassemble the two peptides, we dissolved each peptide in 1,1,1,3,3,3-hexafluoro-2-propanol (HFP) and diluted them in 50% ethanol. The polarized solvent allowed the selfassembly of peptides.
Conc	1mg/ml (1st dipeptide) + 1mg/ml )2nd dipeptide
Temperature	~ 4.5
Temperature	Room temperature
Incubation Time	10 -24 hours
Year	2012
Self assembly	Yes
Type of Self assembly	spherical structures
Tertiary Structure (Technique)	Not Predicted),
	Linear
	Co-assembly of two dipeptides
	Stable upto at 70°C
	Nanosphere
	800
	FF
	N.A.

Primary information
SAPdb ID	1303,
PMID	23061818
Peptide Name	Boc-Phe-Phe-OH and NH2-Phe-Phe-OH
Peptide sequence	FF
N-Terminal Modification	Boc (t-butoxycarbonyl) on 1st dipeptide
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Mixture
Conjugate partner	Boc-Phe-Phe-OH + NH2-Phe-Phe-OH
Technique	SEM (Scanning Electron Microscopy), HR - SEM (High Resolution Scanning Electron Microscopy), TEM (Transmission Electron Microscopy), AFM (Atomic force Microscopy)
Solvent	HFP (1,1,1,3,3,3-hexafluoro-2-propanol) + 50% ethanol + 16 mMNaCl
Method	To coassemble the two peptides, we dissolved each peptide in 1,1,1,3,3,3-hexafluoro-2-propanol (HFP) and diluted them in 50% ethanol. The polarized solvent allowed the selfassembly of peptides.
Conc	2mg/ml (1st dipeptide) + 2mg/ml )2nd dipeptide
Temperature	~ 4.5
Temperature	Room temperature
Incubation Time	10 -24 hours
Year	2012
Self assembly	Yes
Type of Self assembly	spherical structures
Tertiary Structure (Technique)	Not Predicted),
	Linear
	Co-assembly of two dipeptides
	Stable upto at 70°C
	Nanosphere
	800
	FF
	N.A.

Primary information
SAPdb ID	1304,
PMID	23061818
Peptide Name	Boc-Phe-Phe-OH and NH2-Phe-Phe-OH
Peptide sequence	FF
N-Terminal Modification	Boc (t-butoxycarbonyl) on 1st dipeptide
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Mixture
Conjugate partner	Boc-Phe-Phe-OH + NH2-Phe-Phe-OH
Technique	SEM (Scanning Electron Microscopy), HR - SEM (High Resolution Scanning Electron Microscopy), TEM (Transmission Electron Microscopy), AFM (Atomic force Microscopy)
Solvent	HFP (1,1,1,3,3,3-hexafluoro-2-propanol) + 50% ethanol + 16 mMNaCl
Method	To coassemble the two peptides, we dissolved each peptide in 1,1,1,3,3,3-hexafluoro-2-propanol (HFP) and diluted them in 50% ethanol. The polarized solvent allowed the selfassembly of peptides.
Conc	3mg/ml (1st dipeptide) + 3mg/ml )2nd dipeptide
Temperature	~ 4.5
Temperature	Room temperature
Incubation Time	10 -24 hours
Year	2012
Self assembly	Yes
Type of Self assembly	Necklaces like Nanostructue
Tertiary Structure (Technique)	Not Predicted),
	Linear
	Co-assembly of two dipeptides
	Unstable at 70°C
	Others
	550
	FF
	N.A.

Primary information
SAPdb ID	1305,
PMID	23061818
Peptide Name	Boc-Phe-Phe-OH and NH2-Phe-Phe-OH
Peptide sequence	FF
N-Terminal Modification	Boc (t-butoxycarbonyl) on 1st dipeptide
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Mixture
Conjugate partner	Boc-Phe-Phe-OH + NH2-Phe-Phe-OH
Technique	SEM (Scanning Electron Microscopy), HR - SEM (High Resolution Scanning Electron Microscopy), TEM (Transmission Electron Microscopy), AFM (Atomic force Microscopy)
Solvent	HFP (1,1,1,3,3,3-hexafluoro-2-propanol) + 50% ethanol + 16 mMNaCl
Method	To coassemble the two peptides, we dissolved each peptide in 1,1,1,3,3,3-hexafluoro-2-propanol (HFP) and diluted them in 50% ethanol. The polarized solvent allowed the selfassembly of peptides.
Conc	4mg/ml (1st dipeptide) +4mg/ml )2nd dipeptide
Temperature	~ 4.5
Temperature	Room temperature
Incubation Time	10 -24 hours
Year	2012
Self assembly	Yes
Type of Self assembly	Necklaces like Nanostructue
Tertiary Structure (Technique)	Not Predicted),
	Linear
	Co-assembly of two dipeptides
	Unstable at 70°C
	Others
	550
	FF
	N.A.

Primary information
SAPdb ID	1306,
PMID	23061818
Peptide Name	Boc-Phe-Phe-OH and NH2-Phe-Phe-OH
Peptide sequence	FF
N-Terminal Modification	Boc (t-butoxycarbonyl) on 1st dipeptide
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Mixture
Conjugate partner	Boc-Phe-Phe-OH + NH2-Phe-Phe-OH
Technique	SEM (Scanning Electron Microscopy), HR - SEM (High Resolution Scanning Electron Microscopy), TEM (Transmission Electron Microscopy), AFM (Atomic force Microscopy)
Solvent	HFP (1,1,1,3,3,3-hexafluoro-2-propanol) + 50% ethanol + 16 mMNaCl
Method	To coassemble the two peptides, we dissolved each peptide in 1,1,1,3,3,3-hexafluoro-2-propanol (HFP) and diluted them in 50% ethanol. The polarized solvent allowed the selfassembly of peptides.
Conc	3mg/ml (1st dipeptide) + 4mg/ml )2nd dipeptide
Temperature	~ 4.5
Temperature	Room temperature
Incubation Time	10 -24 hours
Year	2012
Self assembly	Yes
Type of Self assembly	Necklaces like Nanostructue
Tertiary Structure (Technique)	Not Predicted),
	Linear
	Co-assembly of two dipeptides
	Unstable at 70°C
	Others
	550
	FF
	N.A.

Primary information
SAPdb ID	1307,
PMID	23061818
Peptide Name	Boc-Phe-Phe-OH and NH2-Phe-Phe-OH
Peptide sequence	FF
N-Terminal Modification	Boc (t-butoxycarbonyl) on 1st dipeptide
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Mixture
Conjugate partner	Boc-Phe-Phe-OH + NH2-Phe-Phe-OH
Technique	SEM (Scanning Electron Microscopy), HR - SEM (High Resolution Scanning Electron Microscopy), TEM (Transmission Electron Microscopy), AFM (Atomic force Microscopy)
Solvent	HFP (1,1,1,3,3,3-hexafluoro-2-propanol) + 50% ethanol + 16 mMNaCl
Method	To coassemble the two peptides, we dissolved each peptide in 1,1,1,3,3,3-hexafluoro-2-propanol (HFP) and diluted them in 50% ethanol. The polarized solvent allowed the selfassembly of peptides.
Conc	3mg/ml (1st dipeptide) + 5mg/ml )2nd dipeptide
Temperature	~ 4.5
Temperature	Room temperature
Incubation Time	10 -24 hours
Year	2012
Self assembly	Yes
Type of Self assembly	Necklaces like Nanostructue
Tertiary Structure (Technique)	Not Predicted),
	Linear
	Co-assembly of two dipeptides
	Unstable at 70°C
	Others
	550
	FF
	N.A.

Primary information
SAPdb ID	1308,
PMID	23061818
Peptide Name	Boc-Phe-Phe-OH and NH2-Phe-Phe-OH
Peptide sequence	FF
N-Terminal Modification	Boc (t-butoxycarbonyl) on 1st dipeptide
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Mixture
Conjugate partner	Boc-Phe-Phe-OH + NH2-Phe-Phe-OH
Technique	SEM (Scanning Electron Microscopy), HR - SEM (High Resolution Scanning Electron Microscopy), TEM (Transmission Electron Microscopy), AFM (Atomic force Microscopy)
Solvent	HFP (1,1,1,3,3,3-hexafluoro-2-propanol) + 50% ethanol + 16 mMNaCl
Method	To coassemble the two peptides, we dissolved each peptide in 1,1,1,3,3,3-hexafluoro-2-propanol (HFP) and diluted them in 50% ethanol. The polarized solvent allowed the selfassembly of peptides.
Conc	5mg/ml (1st dipeptide) + 4mg/ml )2nd dipeptide
Temperature	~ 4.5
Temperature	Room temperature
Incubation Time	10 -24 hours
Year	2012
Self assembly	Yes
Type of Self assembly	Necklaces like Nanostructue
Tertiary Structure (Technique)	Not Predicted),
	Linear
	Co-assembly of two dipeptides
	Unstable at 70°C
	Others
	550
	FF
	N.A.

Primary information
SAPdb ID	1329,
PMID	23708750
Peptide Name	Fc-Phe-Phe-OMe
Peptide sequence	FF
N-Terminal Modification	Ferrocene
C-Terminal Modification	Methoxy
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide derivative
Technique	SEM (Scanning Electron Microscopy) and TEM (Transmission Electron Microscopy)
Solvent	HFP (1,1,1,3,3,3-hexafluoro-2-propanol) + Methanol
Method	Fc-Phe–Phe-OMe was dissolved in 1,1,1,3,3,3-hexafluoro-2-propanol to produce a 100mg/mL stock solution. This solution was diluted with methanol to a concentration 2mg/mL. Nanowires produced upon evaporation of thes olvent at room temperature.
Conc	2mg/ml
Temperature	Room temperature
Year	2013
Self assembly	Yes
Type of Self assembly	Nanowire
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable
	Nanowire
	7500
	FF
	N.A.

Primary information
SAPdb ID	1330,
PMID	23706149
Peptide Name	Phe-Phe
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy)
Solvent	Etahnol
Method	2mg of Peptide dissolved in 0.9 mL of ethanol at 70 °C for 10 min and then cooled to room temperature. To the peptide solution was then added 100 μLaliquot amounts of AuNPs (i.e., spherical, rod, or cage) dispersed in ethanol. After 3−4 h, each peptide−AuNP mixture (100 μL) was placed onto a glass slide or silicon wafer surfaces and dried at ambient temperature, until the solvent evaporated. The resultant dipeptide structures were characterized by SEM.
Conc	2mg/ml
Temperature	Room temperature
Incubation Time	3 - 4 hours
Year	2013
Self assembly	Yes
Type of Self assembly	Randomly ordered , dense tubular Nanostructures
Tertiary Structure (Technique)	Not Predicted),
	Linear
	Laser triggered and In presence of gold nanoparticle of 5 - 10 nm sized
	NA
	Nanoparticle
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1331,
PMID	23706149
Peptide Name	Phe-Phe
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy)
Solvent	Etahnol
Method	2mg of Peptide dissolved in 0.9 mL of ethanol at 70 °C for 10 min and then cooled to room temperature. To the peptide solution was then added 100 μLaliquot amounts of AuNPs (i.e., spherical, rod, or cage) dispersed in ethanol. After 3−4 h, each peptide−AuNP mixture (100 μL) was placed onto a glass slide or silicon wafer surfaces and dried at ambient temperature, until the solvent evaporated. The resultant dipeptide structures were characterized by SEM.
Conc	2mg/ml
Temperature	Room temperature
Incubation Time	4 - 4 hours
Year	2013
Self assembly	Yes
Type of Self assembly	Star like morpholgy
Tertiary Structure (Technique)	Not Predicted),
	Linear
	Laser triggered and In presence of gold nanoparticle of 5 - 10 nm sized
	NA
	Others
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1332,
PMID	23706149
Peptide Name	Phe-Phe
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy)
Solvent	HFIP (1,1,1,3,3,3-hexafluoro-2-Isopropanol)+Chloroform
Method	0.40 M stock Phe−Phe solution was first prepared in 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) and then diluted chloroform to give a final concentration of 8.0 mM. Allow to keep at room temperature
Conc	8mM
Temperature	Room temperature
Year	2013
Self assembly	Yes
Type of Self assembly	Organogel (Thick fibers)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Organogel
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1333,
PMID	23706149
Peptide Name	Phe-Phe
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy)
Solvent	HFIP (1,1,1,3,3,3-hexafluoro-2-Isopropanol)+Chloroform
Method	0.40 M stock Phe−Phe solution was first prepared in 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) and then diluted by AuNPs containing chloroform (3.0 × 1010 to 5.6 × 1011 particles/mL) to give a final concentration of 8.0 mM. allow to keep at room temperature.
Conc	8mM
Temperature	Room temperature
Year	2013
Self assembly	Yes
Type of Self assembly	Organogel (Small fibres with varying length))
Tertiary Structure (Technique)	Not Predicted),
	Linear
	In presence of gold nanoparticles
	NA
	Organogel
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1355,
PMID	24036697
Peptide Name	CDP or H–Phe–Phe–NH2. HCl
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Amidation
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	Co-assemble with azobenzed molecule i.e. CPABS (4-[(3-carboxyl-4-hydroxy)phenylazo]benzenesulfonic acid)
Technique	SEM (Scanning Electron Microscopy)
Solvent	HFIP (1,1,1,3,3,3-hexafluoro-2-Isopropanol) + water
Method	Peptide added to water and to dissolve peptide in solutioh 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) added. Upon adding aqueous solutions of azobenzenes i.e . CPABS to HFIP solution of CDP (in a 1 : 1 mole ratio) at room temperature, yellow precipitates formed rapidly, indicating generation of co-assembled nanostructures.
Temperature	Room temperature
Incubation Time	Several hours
Year	2013
Self assembly	Yes
Type of Self assembly	Microsphere
Tertiary Structure (Technique)	Not Predicted),
	Linear
	Coassembly with Azobenzene
	NA
	Others
	2500
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N

Primary information
SAPdb ID	1356,
PMID	24036697
Peptide Name	CDP or H–Phe–Phe–NH2. HCl
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Amidation
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	Co-assemble with HPABS (4-[(4-hydroxy)phenylazo]benzenesulfonic acid)
Technique	SEM (Scanning Electron Microscopy)
Solvent	HFIP (1,1,1,3,3,3-hexafluoro-2-Isopropanol) + water
Method	Peptide added to water and to dissolve peptide in solutioh 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) added. Upon adding aqueous solutions of azobenzenes i.e . CPABS to HFIP solution of CDP (in a 1 : 1 mole ratio) at room temperature, yellow precipitates formed rapidly, indicating generation of co-assembled nanostructures.
Temperature	Room temperature
Incubation Time	Several hours
Year	2013
Self assembly	Yes
Type of Self assembly	Flower like Nanostructures
Tertiary Structure (Technique)	Not Predicted),
	Linear
	Coassembly with Azobenzene
	NA
	Others
	15000
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N

Primary information
SAPdb ID	1357,
PMID	24036697
Peptide Name	CDP or H–Phe–Phe–NH2. HCl
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Amidation
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	Co-assemble with MO (Methyl orange)
Technique	SEM (Scanning Electron Microscopy)
Solvent	HFIP (1,1,1,3,3,3-hexafluoro-2-Isopropanol) + water
Method	Peptide added to water and to dissolve peptide in solutioh 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) added. Upon adding aqueous solutions of azobenzenes i.e . CPABS to HFIP solution of CDP (in a 1 : 1 mole ratio) at room temperature, yellow precipitates formed rapidly, indicating generation of co-assembled nanostructures.
Temperature	Room temperature
Incubation Time	Several hours
Year	2013
Self assembly	Yes
Type of Self assembly	Plate like Nanostructure
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Others
	2000
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N

Primary information
SAPdb ID	1383,
PMID	24611281
Peptide Name	Diphenylalanine
Peptide sequence	FF
N-Terminal Modification	Fmoc(fluorenylmethoxycarbonyl)
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide derivative
Technique	AFM (Atomic Force Microscopy
Solvent	HFIP (1,1,1,3,3,3-hexafluoro-2-Isopropanol)
Method	Solutions (0.5 mg/ml) of Phe-Phe in HFIP prepared . This solution was used to spin cast dipeptide molecules onto the mica substrate. Spin casting was performed drop dropwise at 1000rpm. But instead of casting mica Dendritic structure formed on mica surface.
Conc	0.5mg/ml
Temperature	20°C
Incubation Time	24 hours
Year	2014
Self assembly	Yes
Type of Self assembly	Dendritic patterns of Nanofibers
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable under ambient conditions atleast for 4 months
	Nanofibers
	NA
	FF
	N.A.

Primary information
SAPdb ID	1404,
PMID	25155031
Peptide Name	Diphenylalanine
Peptide sequence	FF
N-Terminal Modification	Fmoc(fluorenylmethoxycarbonyl)
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide derivative
Technique	TEM (Transmission Electron Microscopy)
Solvent	DMSO + Water (in non-equilibrium phase)
Method	Peptide(1mg) was dissolved in DMSO at selected concentrations, followed by sample was mixed for 1–2 minutes until the solid was fully dissolved in the solvent. Gelation of the samples was triggered by the addition of water at various ratios in order to obtain the desired nal concentration.
Temperature	Room temperature
Incubation Time	< 5 minutes
Year	2014
Self assembly	Yes
Type of Self assembly	Spherical clusters
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanosphere
	2000
	FF
	N.A.

Primary information
SAPdb ID	1405,
PMID	25155031
Peptide Name	Diphenylalanine
Peptide sequence	FF
N-Terminal Modification	Fmoc(fluorenylmethoxycarbonyl)
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide derivative
Technique	TEM (Transmission Electron Microscopy)
Solvent	DMSO + Water (in equilibrium phase)
Method	Peptide(1mg) was dissolved in DMSO at selected concentrations, followed by sample was mixed for 1–2 minutes until the solid was fully dissolved in the solvent. Gelation of the samples was triggered by the addition of water at various ratios in order to obtain the desired nal concentration.
Temperature	Room temperature
Incubation Time	> 5 - 30 minutes
Year	2014
Self assembly	Yes
Type of Self assembly	Nanofibers
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanofibers
	7.5
	FF
	N.A.

Primary information
SAPdb ID	1407,
PMID	25229206
Peptide Name	NDI-Phe-Phe or 1
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Mixture
Conjugate partner	NDI : 1,4,5,8-naphthalenetetracarboxylic acid diimide
Technique	TEM (Transmission Electron Microscopy)
Solvent	Water
Method	2mg compound was dissolved in 0.2ml solvent by heating. Gelation occur at room temperature.
Conc	2% wt
Temperature	pH 4.8
Temperature	Room temperature
Year	2014
Self assembly	Yes
Type of Self assembly	Hydrogel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable
	Hydrogel
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1411,
PMID	25229206
Peptide Name	NDI-Phe-Phe or 1
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Mixture
Conjugate partner	NDI : 1,4,5,8-naphthalenetetracarboxylic acid diimide
Technique	TEM (Transmission Electron Microscopy)
Solvent	Water
Method	2mg compound was dissolved in 0.2ml solvent by heating. Gelation occur at room temperature.
Conc	2% wt
Temperature	pH 7.4
Temperature	Room temperature
Year	2014
Self assembly	Yes
Type of Self assembly	Semitranslucent Hydrogel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable
	Hydrogel
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1415,
PMID	25391268
Peptide Name	Boc-diphenylalanine
Peptide sequence	FF
N-Terminal Modification	Boc (t-butoxycarbonyl)
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	HR - SEM (High Resolution Scanning Electron Microscopy) and DLS (Dynamic light scattering)
Solvent	10% ethanol in water
Method	Dipeptide dissolved in 10% ethanol( in water) at conc 0.2 - 10mg/ml in a vial. Vial sealed to avoid evaporation and allowed to equilibrate for 1 h prior to measurement.
Conc	0.2 - 10mg/ml
Temperature	Room temperature
Incubation Time	< 20 minutes
Year	2014
Self assembly	Yes
Type of Self assembly	Spherical structures
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Transient stable
	Nanosphere
	NA
	FF
	N.A.

Primary information
SAPdb ID	1416,
PMID	25391268
Peptide Name	Boc-diphenylalanine
Peptide sequence	FF
N-Terminal Modification	Boc (t-butoxycarbonyl)
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	HR - SEM (High Resolution Scanning Electron Microscopy) and DLS (Dynamic light scattering)
Solvent	10% ethanol in water
Method	Dipeptide dissolved in 10% ethanol( in water) at conc 0.2 - 10mg/ml in a vial. Vial sealed to avoid evaporation and allowed to equilibrate for 1 h prior to measurement.
Conc	0.2 - 10mg/ml
Temperature	Room temperature
Incubation Time	30 - 40 minutes
Year	2014
Self assembly	Yes
Type of Self assembly	Fibril Nanostructure
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Transient stable
	Nanofibers
	30
	FF
	N.A.

Primary information
SAPdb ID	1417,
PMID	25391268
Peptide Name	Boc-diphenylalanine
Peptide sequence	FF
N-Terminal Modification	Boc (t-butoxycarbonyl)
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	HR - SEM (High Resolution Scanning Electron Microscopy) and DLS (Dynamic light scattering)
Solvent	10% ethanol in water
Method	Dipeptide dissolved in 10% ethanol( in water) at conc 0.2 - 10mg/ml in a vial. Vial sealed to avoid evaporation and allowed to equilibrate for 1 h prior to measurement.
Conc	0.2 - 10mg/ml
Temperature	Room temperature
Incubation Time	60 minutes
Year	2014
Self assembly	Yes
Type of Self assembly	Nanotube
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable
	Nanotube
	NA
	FF
	N.A.

Primary information
SAPdb ID	1441,
PMID	23566763
Peptide Name	Fmoc-FF
Peptide sequence	FF
N-Terminal Modification	Fmoc(fluorenylmethoxycarbonyl)
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy) and DLS (Dynamic Light Scattering)
Solvent	DMSO + water + vitamin E-TPGS
Method	Peptide dissolved in water at concentration of 10 mg/mL. The resulting solution was added drop-wise into 50 mL slightly warmed ( 35 °C) mineral oil containing vitamin E-TPGS atconcentration of 0.4% wt/v and homogenized . Next, nanoparticles were allowed to self-assemble for 2 h with continues stirring at 4 °C. After completion the self assembly process, the resulting suspension was mixed with hexane at a concentration of 20% (v/v), and centrifuged to obtain self assembled nanoparticle.
Conc	10mg/ml
Temperature	4 °C
Incubation Time	2 hours
Year	2013
Self assembly	Yes
Type of Self assembly	Hydrogel Nanoparticle (HNP)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable under physiological conditions
	Hydrogel
	100
	FF
	N.A.

Primary information
SAPdb ID	1451,
PMID	24301009
Peptide Name	NH2-Phe-Phe-OH
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	TEM (Transmission Electron Microscopy), SEM (Scanning Electron Microscopy) and AFM (Atomic Force Microscopy)
Solvent	HFP (1,1,1,3,3,3-hexafluoro-2-propanol) + water
Method	Peptide dissolved in HFP at conc 100mg/ml and solution is vortexed. Finally solution is diluted with water at final conc 2mg/ml. Solution is kept at room temperature for 24 hours.
Conc	2mg/ml
Temperature	Room temperature
Incubation Time	24 hours
Year	2013
Self assembly	Yes
Type of Self assembly	Nanotube
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanotube
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1452,
PMID	24301009
Peptide Name	Boc-Phe-Phe-COOH
Peptide sequence	FF
N-Terminal Modification	Boc (t-butoxycarbonyl)
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	TEM (Transmission Electron Microscopy), SEM (Scanning Electron Microscopy) and AFM (Atomic Force Microscopy)
Solvent	HFP (1,1,1,3,3,3-hexafluoro-2-propanol) + Ethanol
Method	Peptide dissolved in HFP at conc 100mg/ml and solution is vortexed. Finally solution is diluted with ethanol at final conc 2mg/ml. Solution is kept at room temperature for 24 hours.
Conc	5mg/ml
Temperature	Room temperature
Incubation Time	24 hours
Year	2013
Self assembly	Yes
Type of Self assembly	Nanosphere
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanosphere
	NA
	FF
	N.A.

Primary information
SAPdb ID	1453,
PMID	24301009
Peptide Name	NH2-Phe-Phe-OH + Boc-Phe-Phe-COOH
Peptide sequence	FF
N-Terminal Modification	Boc (t-butoxycarbonyl) at 2nd dipeptide
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Mixture
Conjugate partner	Mixture of two dipeptides
Technique	TEM (Transmission Electron Microscopy), SEM (Scanning Electron Microscopy) and AFM (Atomic Force Microscopy)
Solvent	HFP+50 % Ethanol
Method	Peptide dissolved in HFP at conc 100mg/ml and solution is vortexed. Finally solution is diluted with ethanol at final conc 2mg/ml. Solution is kept at room temperature for 24 hours.
Conc	5mg/ml (1st dipeptide) and 3mg/ml (2nd dipeptide)
Temperature	Room temperature
Incubation Time	24 hours
Year	2013
Self assembly	Yes
Type of Self assembly	Necklaces like Nanostructue
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Others
	NA
	FF
	N.A.

Primary information
SAPdb ID	1454,
PMID	24422499
Peptide Name	Diphenylalanine
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy)
Solvent	Isopropanol
Method	Peptide supersaturated solution placed on a glass slide and solutions in various solvents were placed on a glass slide and were left to dry at room temperature.
Conc	2.6 x 10 -4 M
Temperature	Room temperature
Incubation Time	24 - 48 hours
Year	2014
Self assembly	Yes
Type of Self assembly	Lamellar
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Others
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1455,
PMID	24422499
Peptide Name	Diphenylalanine
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy)
Solvent	Formamide solution
Method	Peptide supersaturated solution placed on a glass slide and solutions in various solvents were placed on a glass slide and were left to dry at room temperature.
Conc	2.6 x 10 -4 M
Temperature	Room temperature
Incubation Time	24 - 48 hours
Year	2014
Self assembly	Yes
Type of Self assembly	Translucent gel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1456,
PMID	24889029
Peptide Name	Peptide 1 or H-Phe(4-azido)-Phe(4-azido)-OH
Peptide sequence	FF
N-Terminal Modification	4-azido
C-Terminal Modification	4-azido
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide derivative
Technique	HR - SEM (High Resolution - Scanning Electron Microscopy), STEM (Scanning Transmission Electron Microscopy) and AFM (Atomic Force Microscopy)
Solvent	50% ethanol
Method	Stock solution of dipeptide prepared in HFP at conc 100mg/ml. Peptide solution is diluted with 50 % ethanol in final concentration of 5mg/ml. peptide solution kept in dark at room temperature for 24 hours.
Conc	5mg/ml
Temperature	Room temperature
Incubation Time	24 hours
Year	2014
Self assembly	Yes
Type of Self assembly	Spherical and porous structure
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable
	Others
	1150
	FF
	N.A.

Primary information
SAPdb ID	1457,
PMID	24889029
Peptide Name	Peptide 2 or H-Phe-Phe(4-azido)-OH
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	4-azido
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide derivative
Technique	HR - SEM (High Resolution - Scanning Electron Microscopy), STEM (Scanning Transmission Electron Microscopy) and AFM (Atomic Force Microscopy)
Solvent	50% ethanol
Method	Stock solution of dipeptide prepared in HFP at conc 100mg/ml. Peptide solution is diluted with 50 % ethanol in final concentration of 5mg/ml. peptide solution kept in dark at room temperature for 24 hours.
Conc	5mg/ml
Temperature	Room temperature
Incubation Time	24 hours
Year	2014
Self assembly	No
Type of Self assembly	No assembled structure
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	None
	NA
	FF
	N.A.

Primary information
SAPdb ID	1458,
PMID	24889029
Peptide Name	Peptide 3 or H-Phe(4-azido)-Phe-OH
Peptide sequence	FF
N-Terminal Modification	4-azido
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide derivative
Technique	HR - SEM (High Resolution - Scanning Electron Microscopy), STEM (Scanning Transmission Electron Microscopy) and AFM (Atomic Force Microscopy)
Solvent	50% ethanol
Method	Stock solution of dipeptide prepared in HFP at conc 100mg/ml. Peptide solution is diluted with 50 % ethanol in final concentration of 5mg/ml. peptide solution kept in dark at room temperature for 24 hours.
Conc	5mg/ml
Temperature	Room temperature
Incubation Time	24 hours
Year	2014
Self assembly	No
Type of Self assembly	No assembled structure
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	None
	NA
	FF
	N.A.

Primary information
SAPdb ID	1459,
PMID	24889029
Peptide Name	Peptide 1 or H-Phe(4-azido)-Phe(4-azido)-OH
Peptide sequence	FF
N-Terminal Modification	4-azido
C-Terminal Modification	4-azido
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide derivative
Technique	HR - SEM (High Resolution - Scanning Electron Microscopy), STEM (Scanning Transmission Electron Microscopy) and AFM (Atomic Force Microscopy)
Solvent	TDW (Tripple Distilled Water)
Method	Stock solution of dipeptide prepared in HFP at conc 100mg/ml. Peptide solution is diluted with TDW (Tripple Distilled Water) in final concentration of 5mg/ml. peptide solution kept in dark at room temperature for 24 hours.
Conc	5mg/ml
Temperature	Room temperature
Incubation Time	24 hours
Year	2014
Self assembly	Yes
Type of Self assembly	Spherical and porous structure
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable
	Others
	NA
	FF
	N.A.

Primary information
SAPdb ID	1460,
PMID	24889029
Peptide Name	Peptide 2 or H-Phe-Phe(4-azido)-OH
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	4-azido
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide derivative
Technique	HR - SEM (High Resolution - Scanning Electron Microscopy), STEM (Scanning Transmission Electron Microscopy) and AFM (Atomic Force Microscopy)
Solvent	TDW (Tripple Distilled Water)
Method	Stock solution of dipeptide prepared in HFP at conc 100mg/ml. Peptide solution is diluted with TDW (Tripple Distilled Water) in final concentration of 5mg/ml. peptide solution kept in dark at room temperature for 24 hours.
Conc	5mg/ml
Temperature	Room temperature
Incubation Time	24 hours
Year	2014
Self assembly	Yes
Type of Self assembly	Spherical structure
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable
	Nanosphere
	NA
	FF
	N.A.

Primary information
SAPdb ID	1461,
PMID	24889029
Peptide Name	Peptide 3 or H-Phe(4-azido)-Phe-OH
Peptide sequence	FF
N-Terminal Modification	4-azido
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide derivative
Technique	HR - SEM (High Resolution - Scanning Electron Microscopy), STEM (Scanning Transmission Electron Microscopy) and AFM (Atomic Force Microscopy)
Solvent	TDW (Tripple Distilled Water)
Method	Stock solution of dipeptide prepared in HFP at conc 100mg/ml. Peptide solution is diluted with TDW (Tripple Distilled Water) in final concentration of 5mg/ml. peptide solution kept in dark at room temperature for 24 hours.
Conc	5mg/ml
Temperature	Room temperature
Incubation Time	24 hours
Year	2014
Self assembly	No
Type of Self assembly	No assembled structure
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	None
	NA
	FF
	N.A.

Primary information
SAPdb ID	1462,
PMID	24889029
Peptide Name	Peptide 1 or H-Phe(4-azido)-Phe(4-azido)-OH + Peptide 5 or Boc-Phe-Phe-OH
Peptide sequence	FF
N-Terminal Modification	4-azido
C-Terminal Modification	4-azido
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide derivative
Technique	HR - SEM (High Resolution - Scanning Electron Microscopy), STEM (Scanning Transmission Electron Microscopy) and AFM (Atomic Force Microscopy)
Solvent	50% ethanol
Method	To co-assemble the peptides, both peptides dissolved individually in HFP to a concentration of 100mg/ml. The desired combination of peptides was blended by mixing the peptides in HFP in the desired ratio to form a combination stock solution. The peptide combination stock solution was then diluted to a desired final concentration. peptide solution kept in dark at room temperature for 24 hours.
Conc	5mg/ml of peptide 1, and 3mg/ml of peptide 5
Temperature	Room temperature
Incubation Time	24 hours
Year	2014
Self assembly	Yes
Type of Self assembly	Aggregate of spherical assemblies
Tertiary Structure (Technique)	Not Predicted),
	Linear
	Co-assembly
	NA
	Others
	NA
	FF
	N.A.

Primary information
SAPdb ID	1463,
PMID	24889029
Peptide Name	Peptide 1 or H-Phe(4-azido)-Phe(4-azido)-OH + Peptide 4 or H-Phe-Phe-OH
Peptide sequence	FF
N-Terminal Modification	4-azido
C-Terminal Modification	4-azido
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide derivative
Technique	HR - SEM (High Resolution - Scanning Electron Microscopy), STEM (Scanning Transmission Electron Microscopy) and AFM (Atomic Force Microscopy)
Solvent	50% ethanol
Method	To co-assemble the peptides, both peptides dissolved individually in HFP to a concentration of 100mg/ml. The desired combination of peptides was blended by mixing the peptides in HFP in the desired ratio to form a combination stock solution. The peptide combination stock solution was then diluted to a desired final concentration. peptide solution kept in dark at room temperature for 24 hours.
Conc	5mg/ml of peptide 1, and 3mg/ml of peptide 4
Temperature	Room temperature
Incubation Time	24 hours
Year	2014
Self assembly	Yes
Type of Self assembly	Aggregate of spherical assemblies
Tertiary Structure (Technique)	Not Predicted),
	Linear
	Co-assembly
	NA
	Others
	NA
	FF
	N.A.

Primary information
SAPdb ID	1464,
PMID	24889029
Peptide Name	Peptide 1 or H-Phe(4-azido)-Phe(4-azido)-OH + Peptide 4 or H-Phe-Phe-OH
Peptide sequence	FF
N-Terminal Modification	4-azido
C-Terminal Modification	4-azido
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide derivative
Technique	HR - SEM (High Resolution - Scanning Electron Microscopy), STEM (Scanning Transmission Electron Microscopy) and AFM (Atomic Force Microscopy)
Solvent	TDW (Tripple Distilled Water)
Method	To co-assemble the peptides, both peptides dissolved individually in HFP to a concentration of 100mg/ml. The desired combination of peptides was blended by mixing the peptides in HFP in the desired ratio to form a combination stock solution. The peptide combination stock solution was then diluted to a desired final concentration. peptide solution kept in dark at room temperature for 24 hours.
Conc	5mg/ml of peptide 1, and 3mg/ml of peptide 4
Temperature	Room temperature
Incubation Time	24 hours
Year	2014
Self assembly	Yes
Type of Self assembly	Aggregate of tubular structure
Tertiary Structure (Technique)	Not Predicted),
	Linear
	Co-assembly
	NA
	Others
	NA
	FF
	N.A.

Primary information
SAPdb ID	1465,
PMID	24889029
Peptide Name	Peptide 3 or H-Phe(4-azido)-Phe-OH + Peptide 5 or Boc-Phe-Phe-OH
Peptide sequence	FF
N-Terminal Modification	4-azido
C-Terminal Modification	4-azido
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide derivative
Technique	HR - SEM (High Resolution - Scanning Electron Microscopy), STEM (Scanning Transmission Electron Microscopy) and AFM (Atomic Force Microscopy)
Solvent	50% ethanol
Method	To co-assemble the peptides, both peptides dissolved individually in HFP to a concentration of 100mg/ml. The desired combination of peptides was blended by mixing the peptides in HFP in the desired ratio to form a combination stock solution. The peptide combination stock solution was then diluted to a desired final concentration. peptide solution kept in dark at room temperature for 24 hours.
Conc	5mg/ml of peptide 3, and 3mg/ml of peptide 5
Temperature	Room temperature
Incubation Time	24 hours
Year	2014
Self assembly	Yes
Type of Self assembly	Aggregate of tubular structure
Tertiary Structure (Technique)	Not Predicted),
	Linear
	Co-assembly
	NA
	Others
	NA
	FF
	N.A.

Primary information
SAPdb ID	1466,
PMID	24889029
Peptide Name	Peptide 2 or H-Phe-Phe(4-azido)-OH + Peptide 5 or Boc-Phe-Phe-OH
Peptide sequence	FF
N-Terminal Modification	4-azido
C-Terminal Modification	4-azido
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide derivative
Technique	HR - SEM (High Resolution - Scanning Electron Microscopy), STEM (Scanning Transmission Electron Microscopy) and AFM (Atomic Force Microscopy)
Solvent	50% ethanol
Method	To co-assemble the peptides, both peptides dissolved individually in HFP to a concentration of 100mg/ml. The desired combination of peptides was blended by mixing the peptides in HFP in the desired ratio to form a combination stock solution. The peptide combination stock solution was then diluted to a desired final concentration. peptide solution kept in dark at room temperature for 24 hours.
Conc	5mg/ml of peptide 2, and 3mg/ml of peptide 5
Temperature	Room temperature
Incubation Time	24 hours
Year	2014
Self assembly	Yes
Type of Self assembly	Fused and flat spheres
Tertiary Structure (Technique)	Not Predicted),
	Linear
	Co-assembly
	NA
	Nanosphere
	NA
	FF
	N.A.

Primary information
SAPdb ID	1467,
PMID	24889029
Peptide Name	Peptide 3 or H-Phe(4-azido)-Phe-OH+ Peptide 4 or H-Phe-Phe-OH + Peptide 5 or Boc-Phe-Phe-OH
Peptide sequence	FF
N-Terminal Modification	4-azido
C-Terminal Modification	4-azido
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide derivative
Technique	HR - SEM (High Resolution - Scanning Electron Microscopy), STEM (Scanning Transmission Electron Microscopy) and AFM (Atomic Force Microscopy)
Solvent	50% ethanol
Method	To co-assemble the peptides, both peptides dissolved individually in HFP to a concentration of 100mg/ml. The desired combination of peptides was blended by mixing the peptides in HFP in the desired ratio to form a combination stock solution. The peptide combination stock solution was then diluted to a desired final concentration. peptide solution kept in dark at room temperature for 24 hours.
Conc	0.3mg/ml, 5mg/ml of peptide 4, and 3mg/ml of peptide 5
Temperature	Room temperature
Incubation Time	24 hours
Year	2014
Self assembly	Yes
Type of Self assembly	Necklace like Nanostructure
Tertiary Structure (Technique)	Not Predicted),
	Linear
	Co-assembly
	Unstable
	Others
	NA
	FF
	N.A.

Primary information
SAPdb ID	1481,
PMID	22651803
Peptide Name	Dipeptide9
Peptide sequence	FF
N-Terminal Modification	Napthalene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy) and X - Ray Diffraction
Solvent	Water + 0.1 M NaOH
Method	25mg of dipeptide was suspended in deionized 5ml water . An equimolar amount of NaOH (0.1 M,aq) was added, and the solution was gently stirred until a clear solution was formed. Glucono-δ- lactone (GdL) was added to the solution and the samples were gently swirled to dissolve the GdL before being left to stand for 24 h without stirring to form gel.
Conc	5mg/ml or 0.5%wt
Temperature	Room temperature
Incubation Time	24 hours
Year	2012
Self assembly	Yes
Type of Self assembly	Transparent or clear gel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1486,
PMID	22651803
Peptide Name	Dipeptide18
Peptide sequence	FF
N-Terminal Modification	Napthalene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy) and X - Ray Diffraction
Solvent	Water + 0.1 M NaOH
Method	25mg of dipeptide was suspended in deionized 5ml water . An equimolar amount of NaOH (0.1 M,aq) was added, and the solution was gently stirred until a clear solution was formed. Glucono-δ- lactone (GdL) was added to the solution and the samples were gently swirled to dissolve the GdL before being left to stand for 24 h without stirring to form gel.
Conc	5mg/ml or 0.5%wt
Temperature	Room temperature
Incubation Time	24 hours
Year	2012
Self assembly	Yes
Type of Self assembly	Transparent or clear gel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1494,
PMID	19893524
Peptide Name	cyclo-Phe-Phe
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	SEM (Scanning Electron Microscopy)
Method	1 mg of diphenylalanine peptide lyophilized powder was placed in a small copper boat to serve as the source material. The substrate was placed above the source at a vertical distance of 2 cm. The chamber was then set to 220°C with a heating rate of 10°C per 2min at a constant pressure of 1X10 5mbar. Control of ADNT thickness was achieved by varying the deposition time.
Conc	1mg lyophilized powder
Temperature	220°C
Incubation Time	2 - 10 minutes
Year	2009
Self assembly	Yes
Type of Self assembly	Vertical Nanotube
Tertiary Structure (Technique)	Not Predicted),
	Cyclic
	NA
	Proteolytically stable
	Nanotube
	40000
	FF
	N.A.

Primary information
SAPdb ID	1495,
PMID	19893524
Peptide Name	cyclo-D-Phe-D-Phe
Peptide sequence	ff
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	SEM (Scanning Electron Microscopy)
Method	1 mg of diphenylalanine peptide lyophilized powder was placed in a small copper boat to serve as the source material. The substrate was placed above the source at a vertical distance of 2 cm. The chamber was then set to 220°C with a heating rate of 10°C per 2min at a constant pressure of 1X10 5mbar. Control of ADNT thickness was achieved by varying the deposition time.
Conc	1mg lyophilized powder
Temperature	220°C
Incubation Time	2 - 10 minutes
Year	2009
Self assembly	Yes
Type of Self assembly	Vertical Nanotube
Tertiary Structure (Technique)	Not Predicted),
	Cyclic
	NA
	Proteolytically stable
	Nanotube
	40000
	ff
	N.A.

Primary information
SAPdb ID	1499,
PMID	19198495
Peptide Name	Phe-Phe
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	FE - SEM (Field Emission Scanning Electron Microscopy)
Solvent	Water
Method	Dipeptide dissolved by sonicating for 20 min, subsequently stirring it with a magnetic bar at 60°C and on cooling to room temperature, nanostructures were formed
Conc	4mg/ml
Temperature	Room temperature
Year	2008
Self assembly	Yes
Type of Self assembly	Nanotube
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanotube
	100
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)CO

Primary information
SAPdb ID	1500,
PMID	19198495
Peptide Name	Phe-Phe
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	FE - SEM (Field Emission Scanning Electron Microscopy)
Solvent	Methanol
Method	Dipeptide dissolved by sonicating for 20 min, subsequently stirring it with a magnetic bar at 60°C and on cooling to room temperature, nanostructures were formed
Conc	10mg/ml
Temperature	Room temperature
Year	2008
Self assembly	Yes
Type of Self assembly	Nanoribbon
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanoribbon
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1501,
PMID	19198495
Peptide Name	Phe-Phe
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	FE - SEM (Field Emission Scanning Electron Microscopy)
Solvent	Ethanol
Method	Dipeptide dissolved by sonicating for 20 min, subsequently stirring it with a magnetic bar at 60°C and on cooling to room temperature, nanostructures were formed
Conc	10mg/ml
Temperature	Room temperature
Year	2008
Self assembly	Yes
Type of Self assembly	Nanoribbon
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanoribbon
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1502,
PMID	19198495
Peptide Name	Phe-Phe
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	FE - SEM (Field Emission Scanning Electron Microscopy)
Solvent	Dichloromethane
Method	Dipeptide dissolved by sonicating for 20 min, subsequently stirring it with a magnetic bar at 60°C and on cooling to room temperature, nanostructures were formed
Conc	4mg/ml
Temperature	Room temperature
Year	2008
Self assembly	Yes
Type of Self assembly	Nanoribbon and Nanowires
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanoribbon, Nanowires
	550
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1503,
PMID	20050040
Peptide Name	Hydrogelator 1 (Nap-L-Phe-L-Phe)
Peptide sequence	FF
N-Terminal Modification	Napthalene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	TEM (Transmission Electron Microscopy)
Solvent	Water
Method	10 mg of the hydrogelator dissolves readily in 1.0 mL of pure water at pH = 10, and the hydrogel forms upon adjusting the pH of the solution back to around 7
Conc	10mg/ml
Temperature	7.5
Temperature	Room temperature
Year	2009
Self assembly	Yes
Type of Self assembly	Hydrogel (consists of fibers)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable at room temperature atleast for one month
	Hydrogel
	10000
	FF
	N.A.

Primary information
SAPdb ID	1504,
PMID	20050040
Peptide Name	Hydrogelator 2 (Nap-D-Phe-D-Phe)
Peptide sequence	ff
N-Terminal Modification	Napthalene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	TEM (Transmission Electron Microscopy)
Solvent	Water
Method	10 mg of the hydrogelator dissolves readily in 1.0 mL of pure water at pH = 10, and the hydrogel forms upon adjusting the pH of the solution back to around 7
Conc	10mg/ml
Temperature	7.5
Temperature	Room temperature
Year	2009
Self assembly	Yes
Type of Self assembly	Hydrogel (consists of fibers)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable at room temperature atleast for one month
	Hydrogel
	NA
	ff
	N.A.

Primary information
SAPdb ID	1508,
PMID	20356006
Peptide Name	Phe-Phe
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	FE - SEM (Field Emission Scanning Electron Microscopy)
Solvent	Water + toluene
Method	10 mg of peptide dissolved in 2 mL of water at 50 °C followed byr sonication, and 2 mL of toluene was added to form an organic layer above the water layer. After 10 min, a thin white film formed at the interface. The film was lifted onto quartz or Si substrate for characterization. Time period can be incresded to obtain more denser aggregation.
Conc	5mg/ml
Temperature	50°C for sonication
Incubation Time	10 minutes
Year	2009
Self assembly	Yes
Type of Self assembly	Fibril
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable at upto 350°C
	Nanofibers
	22500
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1509,
PMID	20356006
Peptide Name	Phe-Phe
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	FE - SEM (Field Emission Scanning Electron Microscopy)
Solvent	Water + toluene
Method	10 mg of peptide dissolved in 2 mL of water at 50 °C followed byr sonication, and 2 mL of toluene was added to form an organic layer above the water layer. After 10 min, a thin white film formed at the interface. The film was lifted onto quartz or Si substrate for characterization. Time period can be incresded to obtain more denser aggregation.
Conc	5mg/ml
Temperature	50°C for sonication
Incubation Time	150 minutes
Year	2009
Self assembly	Yes
Type of Self assembly	Fibril
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable at upto 350°C
	Nanofibers
	90000
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1510,
PMID	20461244
Peptide Name	Peptide-I
Peptide sequence	FF
N-Terminal Modification	Napthalene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Solvent	Water + NaOH + 3.75 mg/ml GdL(glucono-delta-lactone)
Method	Addition of NaOH to an aqueous suspension of the dipeptide followed by addition of 3.75 mg mL 1 of GdL resulted in the formation of a transparent gel
Conc	2.2mM
Incubation Time	15 minutes
Year	2010
Self assembly	Yes
Type of Self assembly	Transparent hydrogel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1518,
PMID	20695592
Peptide Name	Dipeptide 6
Peptide sequence	FF
N-Terminal Modification	Napthalene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	TEM (Transmission Electron Microscopy)
Solvent	Water + NaOH + 8.75 mg/ml GdL(glucono-delta-lactone)
Method	Dipeptide solution mixed with equimolar solution of 0.1M NaOH followd by gentle stirring for 30 minutes to obtain clear solution. Then to lower the pH GdL is added and kept it undisturbed for 24 hours to get gel.
Conc	0.5%wt
Temperature	3.4 +/- 0.2.
Temperature	Room temperature
Incubation Time	> 24 hours
Year	2010
Self assembly	Yes
Type of Self assembly	Transparent gel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1524,
PMID	20695592
Peptide Name	Dipeptide 12
Peptide sequence	FF
N-Terminal Modification	Bromo-Napthalene or napthalene derivative
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	TEM (Transmission Electron Microscopy)
Solvent	Water + NaOH + 8.75 mg/ml GdL(glucono-delta-lactone)
Method	Dipeptide solution mixed with equimolar solution of 0.1M NaOH followd by gentle stirring for 30 minutes to obtain clear solution. Then to lower the pH GdL is added and kept it undisturbed for 24 hours to get gel.
Conc	0.5%wt
Temperature	3.4 +/- 0.2.
Temperature	Room temperature
Incubation Time	> 24 hours
Year	2010
Self assembly	Yes
Type of Self assembly	Transparent gel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1530,
PMID	20695592
Peptide Name	Dipeptide 18
Peptide sequence	FF
N-Terminal Modification	Cyano-Napthalene or napthalene derivative
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	TEM (Transmission Electron Microscopy)
Solvent	Water + NaOH + 8.75 mg/ml GdL(glucono-delta-lactone)
Method	Dipeptide solution mixed with equimolar solution of 0.1M NaOH followd by gentle stirring for 30 minutes to obtain clear solution. Then to lower the pH GdL is added and kept it undisturbed for 24 hours to get gel.
Conc	0.5%wt
Temperature	3.4 +/- 0.2.
Temperature	Room temperature
Incubation Time	> 24 hours
Year	2010
Self assembly	Yes
Type of Self assembly	Transparent gel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1535,
PMID	20958029
Peptide Name	FF
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	SEM (Scanning Electron Microscopy) and AFM (Atomic force Microscopy)
Solvent	HFIP (1,1,1,3,3,3-hexafluoro-2-Isopropanol) + Methanol
Method	Peptide dissolved in HFIP at a concentration of 100 mg/mL which further diluted to 2mg/ml in DD Water to form self assembled structure
Conc	2 - 10mg/ml
Year	2010
Self assembly	Yes
Type of Self assembly	PQD (Peptide quantum dots)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Others
	2.12
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1536,
PMID	20958029
Peptide Name	FF
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	SEM (Scanning Electron Microscopy) and AFM (Atomic force Microscopy)
Solvent	HFIP (1,1,1,3,3,3-hexafluoro-2-Isopropanol) + water
Method	Peptide dissolved in HFIP at a concentration of 100 mg/mL which further diluted to 2mg/ml in DD Water to form self assembled structure
Conc	2-5 mg/ml
Year	2010
Self assembly	Yes
Type of Self assembly	Nanotube
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanotube
	50
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1538,
PMID	21132174
Peptide Name	Diphenylalanine
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	SEM (Scanning Electron Microscopy)
Solvent	HFIP (1,1,1,3,3,3-hexafluoro-2-Isopropanol) + water
Method	The stock solution was prepared by dissolving the FF peptide powder in HFP and further with Distilled water to get final conc 2mg/ml and kept for 1day to form nanotube.
Conc	2mg/ml
Temperature	pH 5-6
Incubation Time	24 hours or a day
Year	2010
Self assembly	Yes
Type of Self assembly	Nanotube
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable in acetonitrile and PBS
	Nanotube
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1539,
PMID	21107375
Peptide Name	Dipeptide 1
Peptide sequence	FF
N-Terminal Modification	Fmoc(fluorenylmethoxycarbonyl)
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	AFM (Atomic Force Microscopy) and DLS (Dynamic Light Scattering)
Solvent	Sodium phosphate buffer (pH 8)
Method	Peptide was dissolved in a 1 ml volume of 100 mM sodium phosphate buffer (pH 8) in the presence of varying concentrations of subtilisin (1.25–60.0 ml). The mixture was vortexed (30 s) and sonicated on ice for 20 min , and the low temperature ensures that no enzymatic conversion occurs up to this point. This was followed by heating,ceither in an oil bath or within the spectrophotometer using a temperature-controlled cuvet, at 55° for 60 min to allow enzymatic conversion to occur. The self-assembling system was then allowed to cool to room temperature. The gel samples were then left to stand for periods of 72 h.
Conc	10 mmol/kg
Temperature	8
Temperature	Intial 55°C heating for 1 hour and followed by cooling at room temperature
Incubation Time	72 hour
Year	2010
Self assembly	Yes
Type of Self assembly	Transparent gel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1547,
PMID	21221462
Peptide Name	Phe-Phe
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	TEM (Transmission Electron Microscopy) and DLS (Dynamic Light scattering)
Solvent	HFP (1,1,1,3,3,3-hexafluoro-2-propanol) + water
Method	1mg of a purified peptide in 50 ml of HFIP and by subsequent addition of 1 ml of double distilled water. Samples were aged for 2– 24 hours.
Conc	1 mg/ml
Temperature	Room temperature
Incubation Time	2 -24 hours
Year	2011
Self assembly	Yes
Type of Self assembly	Nanotube
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Thermally stable < 63°C
	Nanotube
	45
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1555,
PMID	21612897
Peptide Name	Fmoc-FF
Peptide sequence	FF
N-Terminal Modification	Fmoc(fluorenylmethoxycarbonyl)
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	AFM (Atomic Force Microscopy)
Solvent	Aqeous solution of HCl (pH ~4)
Conc	0.8 - 2 mg/ml
Temperature	pH 2 -4
Year	2011
Self assembly	Yes
Type of Self assembly	Nanorods
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanorod
	20
	FF
	N.A.

Primary information
SAPdb ID	1559,
PMID	21879773
Peptide Name	Phe-Phe
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	SEM (Scanning Electron Microscopy)
Solvent	Ethanol
Method	Dipeptide was freshly prepared by dissolving the peptides in ethanol at a concentration of 2 or 4 mg/mL at 70 C for 10 min and cooled to room temperature. Each peptide solution (100 μL) was then placed r modified surfaces i.e, silicon surface and dried at ambient temperature until the solvent evaporated.
Conc	2 mg/ml
Year	2011
Self assembly	Yes
Type of Self assembly	Tubular structure
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanotube
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1560,
PMID	21879773
Peptide Name	Phe-Phe
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	SEM (Scanning Electron Microscopy)
Solvent	Ethanol
Method	Dipeptide was freshly prepared by dissolving the peptides in ethanol at a concentration of 2 or 4 mg/mL at 70 C for 10 min and cooled to room temperature. Each peptide solution (100 μL) was then placed r modified surfaces i.e, silicon surface and dried at ambient temperature until the solvent evaporated.
Conc	4mg/ml
Year	2011
Self assembly	Yes
Type of Self assembly	Flower like morphology
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Others
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1561,
PMID	21879773
Peptide Name	Phe-Phe
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	SEM (Scanning Electron Microscopy)
Solvent	Ethanol
Method	Dipeptide was freshly prepared by dissolving the peptides in ethanol at a concentration of 2 or 4 mg/mL at 70 C for 10 min and cooled to room temperature. Each peptide solution (100 μL) was then placed r modified surfaces i.e, AAO surface and dried at ambient temperature until the solvent evaporated.
Conc	2 mg/ml
Year	2011
Self assembly	Yes
Type of Self assembly	Tubular and ribbon like morphology
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanotube, Nanoribbon
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1562,
PMID	21879773
Peptide Name	Phe-Phe
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	SEM (Scanning Electron Microscopy)
Solvent	Ethanol
Method	Dipeptide was freshly prepared by dissolving the peptides in ethanol at a concentration of 2 or 4 mg/mL at 70 C for 10 min and cooled to room temperature. Each peptide solution (100 μL) was then placed r modified surfaces i.e, AAO surface and dried at ambient temperature until the solvent evaporated.
Conc	4mg/ml
Year	2011
Self assembly	Yes
Type of Self assembly	Flower like morphology
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Others
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1563,
PMID	21879773
Peptide Name	Phe-Phe
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	SEM (Scanning Electron Microscopy)
Solvent	Ethanol
Method	Dipeptide was freshly prepared by dissolving the peptides in ethanol at a concentration of 2 or 4 mg/mL at 70 C for 10 min and cooled to room temperature. Each peptide solution (100 μL) was then placed r modified surfaces i.e, PPX films with columnar morphologies and dried at ambient temperature until the solvent evaporated.
Conc	2 - 4mg/ml
Year	2011
Self assembly	Yes
Type of Self assembly	Flakelike peptidic Nanostructures
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Others
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1564,
PMID	21879773
Peptide Name	Phe-Phe
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	SEM (Scanning Electron Microscopy)
Solvent	Ethanol
Method	Dipeptide was freshly prepared by dissolving the peptides in ethanol at a concentration of 2 or 4 mg/mL at 70 C for 10 min and cooled to room temperature. Each peptide solution (100 μL) was then placed r modified surfaces i.e, PPX films with helical morphologies and dried at ambient temperature until the solvent evaporated.
Conc	2 - 4mg/ml
Year	2011
Self assembly	Yes
Type of Self assembly	Transparent thin films
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Others
	200
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1565,
PMID	21948432
Peptide Name	1A
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Conjugate (Nucleopeptide)
Conjugate partner	Nucleobase
Technique	TEM (Transmission Electron Microscopy)
Solvent	Water
Method	Peptide that self-assemble in water to form nanofibers and produce hydrogels at a concentration of 2.0 wt% and a pH value around 5
Conc	2 %wt
Temperature	5
Year	2011
Self assembly	Yes
Type of Self assembly	Hydogel (consists of fibers)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	16
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1566,
PMID	21948432
Peptide Name	1G
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Conjugate (Nucleopeptide)
Conjugate partner	Nucleobase
Technique	TEM (Transmission Electron Microscopy)
Solvent	Water
Method	Peptide that self-assemble in water to form nanofibers and produce hydrogels at a concentration of 2.0 wt% and a pH value around 5
Conc	2 %wt
Temperature	5
Year	2011
Self assembly	Yes
Type of Self assembly	Hydogel (consists of fibers)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	15
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1567,
PMID	21948432
Peptide Name	1T
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Conjugate (Nucleopeptide)
Conjugate partner	Nucleobase
Technique	TEM (Transmission Electron Microscopy)
Solvent	Water
Method	Peptide that self-assemble in water to form nanofibers and produce hydrogels at a concentration of 2.0 wt% and a pH value around 5
Conc	2 %wt
Temperature	5
Year	2011
Self assembly	Yes
Type of Self assembly	Hydogel (consists of fibers)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable
	Hydrogel
	9
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1568,
PMID	21948432
Peptide Name	1C
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Conjugate (Nucleopeptide)
Conjugate partner	Nucleobase
Technique	TEM (Transmission Electron Microscopy)
Solvent	Water
Method	Peptide that self-assemble in water to form nanofibers and produce hydrogels at a concentration of 2.0 wt% and a pH value around 5
Conc	2 %wt
Temperature	5
Year	2011
Self assembly	Yes
Type of Self assembly	Hydogel (consists of fibers)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	10
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1569,
PMID	21948432
Peptide Name	3A
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Conjugate (Nucleopeptide)
Conjugate partner	Nucleobase
Technique	TEM (Transmission Electron Microscopy)
Solvent	Water
Method	Peptide that self-assemble in water to form nanofibers and produce hydrogels at a concentration of 2.0 wt% and a pH value around 7.4
Conc	2 %wt
Temperature	7.4
Year	2011
Self assembly	Yes
Type of Self assembly	Hydogel (consists of fibers)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	20
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1570,
PMID	21948432
Peptide Name	3G
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Conjugate (Nucleopeptide)
Conjugate partner	Nucleobase
Technique	TEM (Transmission Electron Microscopy)
Solvent	Water
Method	Peptide that self-assemble in water to form nanofibers and produce hydrogels at a concentration of 2.0 wt% and a pH value around 7.4
Conc	2 %wt
Temperature	7.4
Year	2011
Self assembly	Yes
Type of Self assembly	Hydogel (consists of fibers)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	14
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1571,
PMID	21948432
Peptide Name	3T
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Conjugate (Nucleopeptide)
Conjugate partner	Nucleobase
Technique	TEM (Transmission Electron Microscopy)
Solvent	Water
Method	Peptide that self-assemble in water to form nanofibers and produce hydrogels at a concentration of 2.0 wt% and a pH value around 7.4
Conc	2 %wt
Temperature	7.4
Year	2011
Self assembly	Yes
Type of Self assembly	Hydogel (consists of fibers)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable
	Hydrogel
	9
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1572,
PMID	21948432
Peptide Name	3C
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Conjugate (Nucleopeptide)
Conjugate partner	Nucleobase
Technique	TEM (Transmission Electron Microscopy)
Solvent	Water
Method	Peptide that self-assemble in water to form nanofibers and produce hydrogels at a concentration of 2.0 wt% and a pH value around 7.4
Conc	2 %wt
Temperature	7.4
Year	2011
Self assembly	Yes
Type of Self assembly	Hydogel (consists of fibers)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	5
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1579,
PMID	22005767
Peptide Name	Peptide 2
Peptide sequence	FF
N-Terminal Modification	Napthalene-nitrile
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	Cryo - TEM (Transmission Electron Microscopy)
Solvent	Water + GdL(glucono-delta-lactone) + Calcium nitrate
Method	0.5wt% dipeptide solution was prepared by adding 200 mg dipeptide into water. The pH was adjusted to 11.7 with the addition of NaOH (1.0 M) solution into the stock solution to form a transparent, viscous solution after mild stirring for 2 hours. To the dipeptide stock solution, 200mg/ml salt solution added and final solution left to stand overnight. Transparent gels were formed
Conc	0.5 % wt
Temperature	11.7
Incubation Time	90 minutes
Year	2011
Self assembly	Yes
Type of Self assembly	Hydrogel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1580,
PMID	22005767
Peptide Name	Peptide 1
Peptide sequence	FF
N-Terminal Modification	Napthalene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	Cryo - TEM (Transmission Electron Microscopy)
Solvent	Water + GdL(glucono-delta-lactone) + Calcium nitrate
Method	0.5wt% dipeptide solution was prepared by adding 200 mg dipeptide into water. The pH was adjusted to 11.7 with the addition of NaOH (1.0 M) solution into the stock solution to form a transparent, viscous solution after mild stirring for 2 hours. To the dipeptide stock solution,200mg/ml salt solution added andfinal solution left to stand overnight. Transparent gels were formed
Conc	0.5 % wt
Temperature	11.7
Incubation Time	90 minutes
Year	2011
Self assembly	Yes
Type of Self assembly	Hydrogel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1581,
PMID	22005767
Peptide Name	Peptide 1
Peptide sequence	FF
N-Terminal Modification	Napthalene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	Cryo - TEM (Transmission Electron Microscopy)
Solvent	Water + GdL(glucono-delta-lactone) + Sodium chloride
Method	0.5wt% dipeptide solution was prepared by adding 200 mg dipeptide into water. The pH was adjusted to 11.3 with the addition of NaOH (1.0 M) solution into the stock solution to form a transparent, viscous solution after mild stirring for 2 hours. To the dipeptide stock solution salt (GdL) solution added andfinal solution left to stand overnight. Transparent gels were formed
Conc	0.5 % wt
Temperature	11.3
Incubation Time	90 minutes
Year	2011
Self assembly	Yes
Type of Self assembly	Hydrogel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1582,
PMID	22005767
Peptide Name	Peptide 1
Peptide sequence	FF
N-Terminal Modification	Napthalene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	Cryo - TEM (Transmission Electron Microscopy)
Solvent	Water + GdL(glucono-delta-lactone) + Lithium chloride
Method	0.5wt% dipeptide solution was prepared by adding 200 mg dipeptide into water. The pH was adjusted to 10.5 with the addition of NaOH (1.0 M) solution into the stock solution to form a transparent, viscous solution after mild stirring for 2 hours. To the dipeptide stock solution, 200mg/ml salt solution added andfinal solution left to stand overnight. Transparent gels were formed
Conc	0.5 % wt
Temperature	10.5
Incubation Time	90 minutes
Year	2011
Self assembly	Yes
Type of Self assembly	Hydrogel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1583,
PMID	22005767
Peptide Name	Peptide 1
Peptide sequence	FF
N-Terminal Modification	Napthalene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	Cryo - TEM (Transmission Electron Microscopy)
Solvent	Water + GdL(glucono-delta-lactone) + Lithium sulphate
Method	0.5wt% dipeptide solution was prepared by adding 200 mg dipeptide into water. The pH was adjusted to 11.7 with the addition of NaOH (1.0 M) solution into the stock solution to form a transparent, viscous solution after mild stirring for 2 hours. To the dipeptide stock solution salt (GdL) solution added andfinal solution left to stand overnight. Transparent gels were formed
Conc	0.5 % wt
Temperature	11.7
Incubation Time	90 minutes
Year	2011
Self assembly	Yes
Type of Self assembly	Hydrogel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1584,
PMID	22005767
Peptide Name	Peptide 1
Peptide sequence	FF
N-Terminal Modification	Napthalene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	Cryo - TEM (Transmission Electron Microscopy)
Solvent	Water + GdL(glucono-delta-lactone) + sodium nitrate
Method	0.5wt% dipeptide solution was prepared by adding 200 mg dipeptide into water. The pH was adjusted to 10.6 with the addition of NaOH (1.0 M) solution into the stock solution to form a transparent, viscous solution after mild stirring for 2 hours. To the dipeptide stock solution salt, 200mg/ml salt solution added andfinal solution left to stand overnight. Transparent gels were formed
Conc	0.5 % wt
Temperature	10.6
Incubation Time	90 minutes
Year	2011
Self assembly	Yes
Type of Self assembly	Hydrogel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1585,
PMID	22005767
Peptide Name	Peptide 1
Peptide sequence	FF
N-Terminal Modification	Napthalene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	Cryo - TEM (Transmission Electron Microscopy)
Solvent	Water + GdL(glucono-delta-lactone) + potassium chloride
Method	0.5wt% dipeptide solution was prepared by adding 200 mg dipeptide into water. The pH was adjusted to 11.7 with the addition of NaOH (1.0 M) solution into the stock solution to form a transparent, viscous solution after mild stirring for 2 hours. To the dipeptide stock solution, 200mg/ml salt solution added andfinal solution left to stand overnight. Transparent gels were formed
Conc	0.5 % wt
Temperature	11.7
Incubation Time	90 minutes
Year	2011
Self assembly	Yes
Type of Self assembly	Hydrogel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1586,
PMID	22005767
Peptide Name	Peptide 1
Peptide sequence	FF
N-Terminal Modification	Napthalene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	Cryo - TEM (Transmission Electron Microscopy)
Solvent	Water + GdL(glucono-delta-lactone) + Ammonium acetate
Method	0.5wt% dipeptide solution was prepared by adding 200 mg dipeptide into water. The pH was adjusted to 8.8 with the addition of NaOH (1.0 M) solution into the stock solution to form a transparent, viscous solution after mild stirring for 2 hours. To the dipeptide stock solution salt (GdL) solution added andfinal solution left to stand overnight. Transparent gels were formed
Conc	0.5 % wt
Temperature	8.8
Incubation Time	90 minutes
Year	2011
Self assembly	Yes
Type of Self assembly	Hydrogel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1587,
PMID	22005767
Peptide Name	Peptide 1
Peptide sequence	FF
N-Terminal Modification	Napthalene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	Cryo - TEM (Transmission Electron Microscopy)
Solvent	Water + GdL(glucono-delta-lactone) + Ammonium chloride
Method	0.5wt% dipeptide solution was prepared by adding 200 mg dipeptide into water. The pH was adjusted to 8.7 with the addition of NaOH (1.0 M) solution into the stock solution to form a transparent, viscous solution after mild stirring for 2 hours. To the dipeptide stock solution, 200mg/ml salt solution added andfinal solution left to stand overnight. Transparent gels were formed
Conc	0.5 % wt
Temperature	8.7
Incubation Time	90 minutes
Year	2011
Self assembly	Yes
Type of Self assembly	Hydrogel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1588,
PMID	22005767
Peptide Name	Peptide 1
Peptide sequence	FF
N-Terminal Modification	Napthalene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	Cryo - TEM (Transmission Electron Microscopy)
Solvent	Water + GdL(glucono-delta-lactone) + Sodium acetate
Method	0.5wt% dipeptide solution was prepared by adding 200 mg dipeptide into water. The pH was adjusted to 11.6 with the addition of NaOH (1.0 M) solution into the stock solution to form a transparent, viscous solution after mild stirring for 2 hours. To the dipeptide stock solution, 200mg/ml salt solution added andfinal solution left to stand overnight. Transparent gels were formed
Conc	0.5 % wt
Temperature	11.6
Incubation Time	90 minutes
Year	2011
Self assembly	Yes
Type of Self assembly	Hydrogel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1589,
PMID	22005767
Peptide Name	Peptide 1
Peptide sequence	FF
N-Terminal Modification	Napthalene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	Cryo - TEM (Transmission Electron Microscopy)
Solvent	Water + GdL(glucono-delta-lactone) + Magnesium sulphate
Method	0.5wt% dipeptide solution was prepared by adding 200 mg dipeptide into water. The pH was adjusted to 10.2 with the addition of NaOH (1.0 M) solution into the stock solution to form a transparent, viscous solution after mild stirring for 2 hours. To the dipeptide stock solution, 6mg/ml salt solution added andfinal solution left to stand overnight. Transparent gels were formed
Conc	0.5 % wt
Temperature	10.2
Incubation Time	90 minutes
Year	2011
Self assembly	Yes
Type of Self assembly	Hydrogel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1590,
PMID	22005767
Peptide Name	Peptide 1
Peptide sequence	FF
N-Terminal Modification	Napthalene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	Cryo - TEM (Transmission Electron Microscopy)
Solvent	Water + GdL(glucono-delta-lactone) + calcium chloride
Method	0.5wt% dipeptide solution was prepared by adding 200 mg dipeptide into water. The pH was adjusted to 11.3 with the addition of NaOH (1.0 M) solution into the stock solution to form a transparent, viscous solution after mild stirring for 2 hours. To the dipeptide stock solution salt (GdL) solution added andfinal solution left to stand overnight. Transparent gels were formed
Conc	0.5 % wt
Temperature	11.3
Incubation Time	90 minutes
Year	2011
Self assembly	Yes
Type of Self assembly	Hydrogel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1591,
PMID	22005767
Peptide Name	Peptide 1
Peptide sequence	FF
N-Terminal Modification	Napthalene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	Cryo - TEM (Transmission Electron Microscopy)
Solvent	Water + GdL(glucono-delta-lactone) + Magnesium nitrate
Method	0.5wt% dipeptide solution was prepared by adding 200 mg dipeptide into water. The pH was adjusted to 9.9 with the addition of NaOH (1.0 M) solution into the stock solution to form a transparent, viscous solution after mild stirring for 2 hours. To the dipeptide stock solution salt (GdL) solution added andfinal solution left to stand overnight. Transparent gels were formed
Conc	0.5 % wt
Temperature	9.9
Incubation Time	90 minutes
Year	2011
Self assembly	Yes
Type of Self assembly	Hydrogel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1592,
PMID	22005767
Peptide Name	Peptide 1
Peptide sequence	FF
N-Terminal Modification	Napthalene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	Cryo - TEM (Transmission Electron Microscopy)
Solvent	Water + GdL(glucono-delta-lactone) + Magnesium Chloride
Method	0.5wt% dipeptide solution was prepared by adding 200 mg dipeptide into water. The pH was adjusted to 9.7 with the addition of NaOH (1.0 M) solution into the stock solution to form a transparent, viscous solution after mild stirring for 2 hours. To the dipeptide stock solution salt (GdL) solution added andfinal solution left to stand overnight. Transparent gels were formed
Conc	0.5 % wt
Temperature	9.7
Incubation Time	90 minutes
Year	2011
Self assembly	Yes
Type of Self assembly	Hydrogel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1593,
PMID	22005767
Peptide Name	Peptide 1
Peptide sequence	FF
N-Terminal Modification	Napthalene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	Cryo - TEM (Transmission Electron Microscopy)
Solvent	Water + GdL(glucono-delta-lactone) + potassium chloride
Method	0.5wt% dipeptide solution was prepared by adding 200 mg dipeptide into water. The pH was adjusted to 11.7 with the addition of NaOH (1.0 M) solution into the stock solution to form a transparent, viscous solution after mild stirring for 2 hours. To the dipeptide stock solution salt (GdL) solution added andfinal solution left to stand overnight. Transparent gels were formed
Conc	0.5 % wt
Temperature	11.7
Incubation Time	90 minutes
Year	2011
Self assembly	Yes
Type of Self assembly	Hydrogel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1595,
PMID	22037699
Peptide Name	Gelator 1
Peptide sequence	FF
N-Terminal Modification	Napthalene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	TEM (Transmission Electron Microscopy)
Solvent	Water
Method	N-terminated dipeptide self-assemble into supramolecular nanofibers in water to form stable hydrogels with the concentration of less than 0.8 wt% and within a relatively narrow pH range (pH = 5.0–6.0).
Conc	0.8 %wt
Temperature	< 5
Year	2011
Self assembly	No
Type of Self assembly	No assembled structure
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	None
	NA
	FF
	N.A.

Primary information
SAPdb ID	1596,
PMID	22037699
Peptide Name	Gelator 2
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Napthalene
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	TEM (Transmission Electron Microscopy)
Solvent	Water
Method	N-terminated dipeptide self-assemble into supramolecular nanofibers in water to form stable hydrogels with the concentration of less than 0.8 wt% and within a relatively narrow pH range (pH = 5.0–6.0).
Conc	0.8 %wt
Temperature	~ 5 - 6
Year	2011
Self assembly	Yes
Type of Self assembly	Hydrogel (Consists of Fibers)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1597,
PMID	22037699
Peptide Name	Gelator 3
Peptide sequence	FF
N-Terminal Modification	Amino-Napthalene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	TEM (Transmission Electron Microscopy)
Solvent	Water
Method	N-terminated dipeptide self-assemble into supramolecular nanofibers in water to form stable hydrogels with the concentration of less than 0.8 wt% and within a relatively narrow pH range (pH = 5.0–6.0).
Conc	0.8 %wt
Temperature	> 6
Year	2011
Self assembly	No
Type of Self assembly	No assembled structure
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	None
	NA
	FF
	N.A.

Primary information
SAPdb ID	1598,
PMID	22037699
Peptide Name	Gelator 2
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Napthalene
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	TEM (Transmission Electron Microscopy)
Solvent	Water
Method	N-terminated dipeptide self-assemble into supramolecular nanofibers in water to form stable hydrogels with the concentration of less than 0.8 wt% and within a relatively narrow pH range (pH = 5.0–6.0).
Conc	0.012
Temperature	~ 5 - 6
Year	2011
Self assembly	Yes
Type of Self assembly	Hydrogel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1599,
PMID	22037699
Peptide Name	Gelator 3
Peptide sequence	FF
N-Terminal Modification	Amino-Napthalene
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	TEM (Transmission Electron Microscopy)
Solvent	Water
Method	N-terminated dipeptide self-assemble into supramolecular nanofibers in water to form stable hydrogels with the concentration of less than 0.8 wt% and within a relatively narrow pH range (pH = 5.0–6.0).
Conc	0.012
Temperature	~ 5 - 6
Year	2011
Self assembly	Yes
Type of Self assembly	Hydrogel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1600,
PMID	22129632
Peptide Name	Fmoc-Phe-Phe
Peptide sequence	FF
N-Terminal Modification	Fmoc(fluorenylmethoxycarbonyl)
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	TEM (Transmission Electron Microscopy)
Solvent	Water + NaOH + GdL(glucono-delta-lactone)
Method	Dipeptide suspended in water and sonicated. NaOH (0.5 M) was added to the suspension until a solution was formed at conc. 15mM. To induce gelation, GdL was added as a powder to a concentration of 4–40 mM. The sample was quickly mixed stored at room temperature to form gel for 72 h.
Conc	15mM
Temperature	3 - 4
Temperature	Room temperature
Incubation Time	72 hour
Year	2012
Self assembly	Yes
Type of Self assembly	Hydrogel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Mechanically less stable
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1601,
PMID	22129632
Peptide Name	Fmoc-Phe-Phe
Peptide sequence	FF
N-Terminal Modification	Fmoc(fluorenylmethoxycarbonyl)
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	TEM (Transmission Electron Microscopy)
Solvent	Water + NaOH + GdL(glucono-delta-lactone)
Method	Dipeptide suspended in water and sonicated. NaOH (0.5 M) was added to the suspension until a solution was formed at conc. 15mM. To induce gelation, GdL was added as a powder to a concentration of 4–40 mM. The sample was quickly mixed stored at -12°C to form gel for 72 h.
Conc	15mM
Temperature	3 - 4
Temperature	(-)12°C
Incubation Time	72 hour
Year	2012
Self assembly	Yes
Type of Self assembly	Cryogel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable
	Others
	NA
	FF
	N.A.

Primary information
SAPdb ID	1610,
PMID	21085503
Peptide Name	Bis(PhePhe) or 5a
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	TEM (Transmission Electron Microscopy)
Solvent	Ethanol
Method	10 mg peptide placed in a test tube, and the solvent was added by microsyringe in 100-500 µL portions. After each addition the mixture was gently heated until the substance dissolved, and was then allowed to cool spontaneously to room temperature and formation of gel. checked by test tube inversion.
Temperature	Room temperature
Incubation Time	Yes
Year	2010
Self assembly	Yes
Type of Self assembly	Entangled tiny fibers
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanofibers
	13
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1612,
PMID	22534735
Peptide Name	FF-nucleotide conjugate
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Conjugate
Conjugate partner	Nucleotide
Technique	TEM (Transmission Electron Microscopy) and AFM (Atomic Force Microscopy)
Solvent	Water
Method	Peptide was dissolved in water at a concentration of 2 mg/ml. this solution was then incubated for 2 h at 37 °C.
Conc	2mg/ml
Temperature	6.5
Temperature	37°C
Incubation Time	Yes
Year	2012
Self assembly	Yes
Type of Self assembly	Spherical structure
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanosphere
	250
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1613,
PMID	22534735
Peptide Name	FF
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	TEM (Transmission Electron Microscopy) and AFM (Atomic Force Microscopy)
Solvent	Water
Method	Peptide was dissolved in water at a concentration of 2 mg/ml. this solution was then incubated for 2 h at 37 °C.
Conc	2mg/ml
Temperature	6.5
Temperature	37°C
Incubation Time	Yes
Year	2012
Self assembly	Yes
Type of Self assembly	Fibrillar structure
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanofibers
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1614,
PMID	22535547
Peptide Name	Diphenylalanine mono-mannose conjugate
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Conjugate
Conjugate partner	Mannose
Technique	SEM (Scanning Electron Microscopy) and AFM (Atomic force Microscopy)
Solvent	Water
Method	Fresh solutions of glycopeptides (1mM) in appropriate solvents were prepared and incubated at 37°C for 24 hours to form self assembled structures.
Conc	1mM
Temperature	37°C
Incubation Time	24 hours
Year	2012
Self assembly	Yes
Type of Self assembly	Tubular structure
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanotube
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)CO

Primary information
SAPdb ID	1615,
PMID	22535547
Peptide Name	Diphenylalanine bis-mannose conjugate
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Conjugate
Conjugate partner	Bis-Mannose linked through lys
Technique	SEM (Scanning Electron Microscopy) and AFM (Atomic force Microscopy)
Solvent	Water
Method	Fresh solutions of glycopeptides (1mM) in appropriate solvents were prepared and incubated at 37°C for 12 hours to form self assembled structures.
Conc	1mM
Temperature	37°C
Incubation Time	12 hours
Year	2012
Self assembly	Yes
Type of Self assembly	Spherical structure
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	More stable
	Nanosphere
	600
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1616,
PMID	22535547
Peptide Name	Thiolated -Diphenylalanine mono-mannose conjugate
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Conjugate
Conjugate partner	Mannose
Technique	SEM (Scanning Electron Microscopy) and AFM (Atomic force Microscopy)
Solvent	50 % aqeous methanol
Method	Fresh solutions of glycopeptides (1mM) in appropriate solvents were prepared and incubated at 37°C for 24 hours to form self assembled structures.
Conc	1mM
Temperature	37°C
Incubation Time	24 hours
Year	2012
Self assembly	Yes
Type of Self assembly	Spherical aggregate
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Less stable
	Others
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)CO

Primary information
SAPdb ID	1617,
PMID	18837544
Peptide Name	Diphenylalanine
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	EFM (Electrostatic Force Microscopy)
Solvent	HFIP (1,1,1,3,3,3-hexafluoro-2-Isopropanol) + water
Method	The peptide solution was prepared by dissolving the lyophilized form of the diphenylalanine in 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) at a final concentration of 100 mg/mL. Peptide stock solution was diluted in distilled water to a final concentration of 2 mg/mL.
Conc	2mg/ml
Year	2008
Self assembly	Yes
Type of Self assembly	Hollow fibers
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanotube
	7
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1624,
PMID	24896538
Peptide Name	Fmoc-FF
Peptide sequence	FF
N-Terminal Modification	Fmoc(fluorenylmethoxycarbonyl)
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	SEM (Scanning Electron Microscopy) and AFM (Atomic force Microscopy)
Solvent	Phosphate buffer
Method	10 mM Fmoc-FF solution was prepared by dissolving 5.32 mg of Fmoc-FF in 1 mL of phosphate buffer solution. Emulsion formed after hand-shaking for 5 s emulsions form in vials. Gel formed in 24 hours on incubation at room temperature.
Conc	10mM
Temperature	8
Temperature	Room temperature
Incubation Time	24 hours
Year	2014
Self assembly	Yes
Type of Self assembly	Gel (consist of Fibrous network)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Hydrogel
	NA
	FF
	N.A.

Primary information
SAPdb ID	1625,
PMID	23795243
Peptide Name	FF
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	Insilico method: MARTINI coarse - grained molecular dynamic
Solvent	Water
Method	A simulation for each dipeptide (in their zwitterionic form) was set up using the GROMACS molecular dynamics package. A cubic box with 300 dipeptides, placed randomly with a minimum distance of 3 Å between them, was solvated in standard MARTINI CG water (four water molecules per bead) to a final concentration of ∼0.4 M. A Berendsen thermostat and barostat36 were used to keep the temperature at 303 K and pressure at 1 bar, respectively. Bond lengths in aromatic side chains and the backbone side-chain bonds in I, V, and Y were constrained using the LINCS algorithm.37 All boxes were energy minimized using the steepest descent integrator and then equilibrated for 4 106 time steps of 25 fs. The total screening simulation time equates to 100 ns, but because of the smoothness of the CG potentials, this roughly equates to an effective 400 ns of atomistic simulation time
Conc	0.4M
Temperature	30°C
Year	2011
Self assembly	Yes
Type of Self assembly	Tubes and Vesicles
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanotube, Nanovesicle
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1634,
PMID	24895323
Peptide Name	Diphenylalanine
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	ESEM (Environmental Scanning Electron Microscope)
Solvent	HFP (1,1,1,3,3,3-hexafluoro-2-propanol)
Method	FF-peptide nanotubes (PNT) were prepared by dissolving the L-diphenylalanine peptide in 1,1,1,3,3,3-hexafluoro-2-propanol an initial concentration of 100mg/ml further diluted in deionized water. Drops of the above solutions at a final concentrationof 2mg/ml were placed onto clean silicon substrates and dried at room temperature. The thermally induced PNT samples were heated in an oven for 180 min at 180 °C.
Conc	2mg/ml
Temperature	Room temperature
Incubation Time	180 minutes
Year	2014
Self assembly	Yes
Type of Self assembly	Nanotubes
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanotube
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O

Primary information
SAPdb ID	1635,
PMID	24895323
Peptide Name	Diphenylalanine
Peptide sequence	FF
N-Terminal Modification	Free
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Conjugate partner	None
Technique	ESEM (Environmental Scanning Electron Microscope)
Solvent	HFP (1,1,1,3,3,3-hexafluoro-2-propanol)
Method	FF-peptide nanotubes (PNT) were prepared by dissolving the L-diphenylalanine peptide in 1,1,1,3,3,3-hexafluoro-2-propanol an initial concentration of 100mg/ml further diluted in deionized water. Drops of the above solutions at a final concentrationof 2mg/ml were placed onto clean silicon substrates and dried at room temperature. The thermally induced PNT samples were heated in an oven for 180 min at 180 °C.
Conc	2mg/ml
Temperature	180 °C
Incubation Time	>180 minutes
Year	2014
Self assembly	Yes
Type of Self assembly	Needle like wire -Nanofibril structure
Tertiary Structure (Technique)	Not Predicted),
	Linear
	Temperature induced
	NA
	Nanofibers, Nanowire
	NA
	FF
	N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O