Details of SAPdb ID 1634 |
| Primary information | ||
|---|---|---|
| SAPdb_ID | 1634 | |
| PMID | 24895323 | |
| Year | 2014 | |
| Name | Diphenylalanine | |
| Sequence | FF | |
| N-Terminal Modification | Free | |
| C-Terminal Modification | Free | |
| Non-terminal Modication | None | |
| Length | 2 | |
| Peptide/Conjugate/Mixture | 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. | |
| Concentration | 2mg/ml | |
| pH | NA | |
| Temperature | Room temperature | |
| Incubation Period | 180 minutes | |
| Self-Assembly Formation | Yes | |
| Type of Self-Assembly | Nanotubes | |
| Size of Self-Assembled structure | NA | |
| Linear/Cyclic | Linear | |
| Stability of Nanostructure | NA | |
| Comment | NA | |
| Secondary information | ||
| Physico-Chemical properties |
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| STRUCTURE |
| |
| SMILES | N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C=O | |