Modifications peptidiques
Peptide cyclique
What is Cyclic Peptide?
Peptide cyclization to form cyclic peptides or cyclized peptides is a frequently used strategy for the development of peptides with enhanced conformational stability compared to their linear analogs. Cyclic peptides have proven to be useful for several applications, including the mimicry of protein secondary structures, such as protein loops, and the optimization of peptide ligands with increased binding potency, sélectivité, and enhanced protease stability.
Cyclization configurations
The primary ligation approaches to synthesize lactam cyclic peptides are head-to-tail, chaîne latérale à chaîne latérale, head-to-side-chain, and side-chain-to-tail,depending on the location of the functional groups within the peptide sequence.

Head to Tail
·Occurs between N-terminus to C-terminus.
·Via Amide bond formation (lactamization).
·Most frequently used cyclization conferring greater stability.

Side Chain to Head
Occurs between N-terminus and an internal COOH
(par exemple. the ß-COOH-group of Asp or γ-COOH-group of Glu).

Side Chain to tail
Occurs between internal NH2s and C-terminus
(par exemple. the ε-NH2–group of Lys).

Side Chain to Side Chain
Occurs between Side chain of Lysine (ε-NH2–group of Lys) to Aspartic or Glutamic acid (γ-COOH-group).
Citations en vedette
Design and NMR Studies of Cyclic Peptides Targeting the N-Terminal Domain of the Protein Tyrosine Phosphatase YopH
We report on the design and evaluation of novel cyclic peptides targeting the N-terminal domain of the protein tyrosine phosphatase YopH from Yersinia. Cyclic peptides have been designed based on a short sequence from the protein SKAP-HOM [DE(pY)DDPF (pY = phosphotyrosine)], and they all contain the motif DEZXDPfK (where Z is a phosphotyrosine or a non-hydrolyzable phosphotyrosine mimetic, X is an aspartic acid or a leucine and f is a d-phenylalanine). These peptides present a ‘head to tail’ architecture, enabling cyclization through formation of an amide bond in between the side chains of the first aspartic acid and the lysine residues. Chemical shift perturbation studies have been carried out to monitor the binding of these peptides to the N-terminal domain of YopH. Peptides containing a phosphotyrosine moiety exhibit binding affinities in the low micromolar range; substitution of the phosphotyrosine with one of its non-hydrolyzable derivatives dramatically reduces the binding affinities. These preliminary studies may pave the way for the discovery of more potent and selective peptidebased ligands of the YopH N-terminal domain which could be further investigated for their ability to inhibit Yersiniae infections.
Services de modification peptidique associés
glycosylation peptidique
glycosylation peptidique
La glycosylation peptidique est une modification covalente qui peut potentiellement améliorer les propriétés physicochimiques des peptides.
En savoir plusPhosphorylation des peptides
Phosphorylation des peptides
Une phosphoralisation peut se produire sur Serine (S, Être), Thréonine (T, Thr) et Tyrosine (Oui, Tyr) chaînes latérales par formation de liaisons phosphoester
En savoir plusPeptides agrafés
Peptides agrafés
Introduction de deux acides aminés non naturels contenant de l'α-méthyle, Groupes α-alcényle lors de la synthèse en phase solide de chaînes peptidiques.
En savoir plusPeptide cyclique
Peptide cyclique
La cyclisation des peptides améliore la stabilité conformationnelle des peptides (par rapport à leurs analogues linéaires) et constitue une stratégie courante dans le développement de peptides.
En savoir plusmodification peptidique
Vaste expérience en modification peptidique, offrant de multiples voies viables pour la recherche sur les peptides.