Peptide (revision 2)
Old revision·03:11, 15 Jun 2024·Chromatokid
| Peptide | |
|---|---|
| Bond | Amide (peptide) bond, C(=O)–NH |
| Conventional upper limit | ≈50 residues, above which "protein" is used |
| Directionality | Written N-terminus to C-terminus |
| Topic infobox · conventions | |
A peptide is a molecule composed of amino acid residues joined by amide bonds formed between the carboxyl group of one residue and the amino group of the next. The boundary with protein is conventional rather than physical; a common cut is around fifty residues, and regulatory definitions differ from chemical usage.[1]
Peptides are directional. By convention a sequence is written from the free amino terminus to the free carboxyl terminus, and the direction is not arbitrary: the same residues in reverse order are a different molecule with different properties. This is the reason a sequence given without its direction is ambiguous.[1]
Structure
[edit]The amide bond has partial double-bond character, which restricts rotation and makes the six atoms of the peptide unit approximately planar. Conformational freedom therefore resides in the two dihedral angles either side of each α-carbon, and it is the accessible combinations of these that give rise to the α-helix, the β-sheet and the turn.[1]
Peptides of fewer than about fifteen residues are usually conformationally disordered in solution, sampling many states; longer chains can adopt a persistent fold. Several of the therapeutic peptides discussed on this wiki are helical over part of their length when bound to their receptor but substantially disordered when free, which matters for how they are analysed and stored.