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Details of SAPdb entry with Sequence GG
Primary information
SAPdb ID 1410,
PMID25229206
Peptide NameNDI-Gly-Gly or 4
Peptide sequenceGG
N-Terminal ModificationFree
C-Terminal ModificationFree
Non-Terminal ModificationNone
Length2
Peptide/ConjuagateMixture
Conjugate partnerNDI : 1,4,5,8-naphthalenetetracarboxylic acid diimide
TechniqueTEM (Transmission Electron Microscopy)
SolventWater
Method2mg compound was dissolved in 0.2ml solvent by heating. Gelation occur at room temperature.
Conc2% wt
TemperaturepH 3.8
TemperatureRoom temperature
Year2014
Self assemblyYes
Type of Self assemblyHydrogel
Tertiary Structure
(Technique)
Not Predicted),
Linear
NA
Stable
Hydrogel
NA
GG
NCC(=O)NCC=O
Primary information
SAPdb ID 1414,
PMID25229206
Peptide NameNDI-Gly-Gly or 4
Peptide sequenceGG
N-Terminal ModificationFree
C-Terminal ModificationFree
Non-Terminal ModificationNone
Length2
Peptide/ConjuagateMixture
Conjugate partnerNDI : 1,4,5,8-naphthalenetetracarboxylic acid diimide
TechniqueTEM (Transmission Electron Microscopy)
SolventWater
Method2mg compound was dissolved in 0.2ml solvent by heating. Gelation occur at room temperature.
Conc2% wt
TemperaturepH 7.4
TemperatureRoom temperature
Year2014
Self assemblyNo
Type of Self assemblyNo gel formation
Tertiary Structure
(Technique)
Not Predicted),
Linear
NA
Stable
None
NA
GG
NCC(=O)NCC=O
Primary information
SAPdb ID 1575,
PMID21995651
Peptide NameFmocGG
Peptide sequenceGG
N-Terminal ModificationFmoc(fluorenylmethoxycarbonyl)
C-Terminal ModificationFree
Non-Terminal ModificationNone
Length2
Peptide/ConjuagatePeptide
Conjugate partnerNone
TechniqueTEM (Transmission Electron Microscopy)
SolventWater + Sodium hydroxide + HCl
MethodFmocdipeptide was suspended in water. Sodium hydroxide (0.5 M) was gradually added to the aqueous suspensions of Fmoc dipeptide until pH 10.5 was reached. The samples were vortexed and sonicated for 1 min to fully dissolve the short peptide amphiphiles. 0.085 M HCl added dropwise to attain desired pH, followed by vortexing and sonication. Sample heated to 75-80 °C fto dissolve the peptide.. The sample was subsequently cooled and maintained at 4 °C for∼12 h (overnight) to promote or maintain gelation.
Conc1- 20 mmlol/L
Temperature< 7.4
TemperatureIntial boiling to 75 -80°C heating for 2 minutes and followed by cooling at 4°C
Incubation Time12 hours
Year2011
Self assemblyYes
Type of Self assemblyHydrogel
Tertiary Structure
(Technique)
Not Predicted),
Linear
NA
Stable
Hydrogel
NA
GG
N.A.
Primary information
SAPdb ID 1576,
PMID21995651
Peptide NameFmocGG
Peptide sequenceGG
N-Terminal ModificationFmoc(fluorenylmethoxycarbonyl)
C-Terminal ModificationFree
Non-Terminal ModificationNone
Length2
Peptide/ConjuagatePeptide
Conjugate partnerNone
TechniqueTEM (Transmission Electron Microscopy)
SolventWater + Sodium hydroxide + HCl
MethodFmocdipeptide was suspended in water. Sodium hydroxide (0.5 M) was gradually added to the aqueous suspensions of Fmoc dipeptide until pH 10.5 was reached. The samples were vortexed and sonicated for 1 min to fully dissolve the short peptide amphiphiles. 0.085 M HCl added dropwise to attain desired pH, followed by vortexing and sonication. Sample heated to 75-80 °C fto dissolve the peptide.. The sample was subsequently cooled and maintained at 4 °C for∼12 h (overnight) to promote or maintain gelation.
Conc1- 20 mmlol/L
Temperature4.6
TemperatureIntial boiling to 75 -80°C heating for 2 minutes and followed by cooling at 4°C
Incubation Time12 hours
Year2011
Self assemblyYes
Type of Self assemblyHydrogel (consists of fibers)
Tertiary Structure
(Technique)
Not Predicted),
Linear
NA
Stable
Hydrogel
3
GG
N.A.
Primary information
SAPdb ID 1602,
PMID22292964
Peptide NameMGG
Peptide sequenceGG
N-Terminal Modificationmeso-methoxyphenylporphyrin
C-Terminal ModificationFree
Non-Terminal ModificationNone
Length2
Peptide/ConjuagatePeptide
Conjugate partnerNone
TechniqueTEM (Transmission Electron Microscopy), DLS (Dynamic Light Scattering) and FLIM (Florescence Lifetime Imaging Microscopy)
SolventWater
MethodStock solutions of MGG porphyrin in DMSO (0.25 mM) were prepared and stored in dark. Samples were prepared by dilution of a small aliquot (<1%) of DMSO stock solution and were left to stabilize overnight.
Conc50 μM
Temperature25 - 45°C
Year2012
Self assemblyYes
Type of Self assemblyRod structure
Tertiary Structure
(Technique)
Not Predicted),
Linear
NA
NA
Nanorod
6500
GG
N.A.
Primary information
SAPdb ID 1603,
PMID22292964
Peptide NameMGG
Peptide sequenceGG
N-Terminal Modificationmeso-methoxyphenylporphyrin
C-Terminal ModificationFree
Non-Terminal ModificationNone
Length2
Peptide/ConjuagatePeptide
Conjugate partnerNone
TechniqueTEM (Transmission Electron Microscopy), DLS (Dynamic Light Scattering) and FLIM (Florescence Lifetime Imaging Microscopy)
SolventWater
MethodStock solutions of MGG porphyrin in DMSO (0.25 mM) were prepared and stored in dark. Samples were prepared by dilution of a small aliquot (<1%) of DMSO stock solution and were left to stabilize overnight.
Conc5μM
Temperature25 - 45°C
Year2012
Self assemblyYes
Type of Self assemblyNanosphere
Tertiary Structure
(Technique)
Not Predicted),
Linear
NA
NA
Nanosphere
80
GG
N.A.
Primary information
SAPdb ID 1604,
PMID22292964
Peptide NameMGG
Peptide sequenceGG
N-Terminal Modificationmeso-methoxyphenylporphyrin
C-Terminal ModificationFree
Non-Terminal ModificationNone
Length2
Peptide/ConjuagatePeptide
Conjugate partnerNone
TechniqueTEM (Transmission Electron Microscopy), DLS (Dynamic Light Scattering) and FLIM (Florescence Lifetime Imaging Microscopy)
SolventWater - 25%ethanol mixture
MethodStock solutions of MGG porphyrin in DMSO (0.25 mM) were prepared and stored in dark. Samples were prepared by dilution of a small aliquot (<1%) of DMSO stock solution and were left to stabilize overnight.
Conc5μM
Temperature25 - 45°C
Year2012
Self assemblyYes
Type of Self assemblySpherical structure
Tertiary Structure
(Technique)
Not Predicted),
Linear
NA
NA
Nanosphere
620
GG
N.A.