Lebetin Peptides, A New Class of Potent Platelet Aggregation Inhibitors: Chemical Synthesis, Biological Activity and NMR Spectroscopic Study
Amor Mosbah, Naziha Marrakchi, Pascal Mansuelle, Soumaya Kouidhi, Ernest Giralt, Mohamed El Ayeb, Gaetan Herbette, Ameur Cherif, Didier Gigmes, Herve Darbon, Kamel Mabrouk,
International Journal of Peptide Research and Therapeutics, 26 21-31 (2020)
Lebetin Peptides, A New Class of Potent Platelet Aggregation Inhibitors: Chemical Synthesis, Biological Activity and NMR Spectroscopic Study
Amor Mosbah, Naziha Marrakchi, Pascal Mansuelle, Soumaya Kouidhi, Ernest Giralt, Mohamed El Ayeb, Gaetan Herbette, Ameur Cherif, Didier Gigmes, Herve Darbon, Kamel Mabrouk,
International Journal of Peptide Research and Therapeutics, 26 21-31 (2020)
Platelets have a well-established role in atherosclerosis and related diseases. Lebetins from the venom of Vipera lebetina, lacking the RGD sequence, emerged as a new family of platelet aggregation inhibitors. However, the interaction sites and precise mechanism between lebetin and its substrate remain unclear. Here, we successfully synthesized two peptide analogs, which differ only by one glycine residue at the N-terminus: lebetin 2 alpha (sL2 alpha residues) and lebetin 2 beta (sL2 beta beta residues) were produced in sufficient quantities for structural and functional studies. NMR structure determination showed that the sL2 alpha peptide adopts a compact ring conformation stabilized by a disulfide bond, from which emerge one loop and two extended regions, the C- and N-termini. Interestingly, two RGD-like motifs were identified in the structure of the peptides, suggesting an anti-platelet aggregation effect of the two isoforms. Indeed, activity was demonstrated on human and rabbit platelet-rich plasma where sL2 alpha and sL2 beta showed more potent inhibitory effect on platelet aggregation compared to the previously described native lebetin 1. Synthetic lebetin 2 peptides constitute promising candidates for drug design toward chimeric compounds with high anti-platelet and natriuretic effects. These findings contribute to a novel field of research triggering platelet activation and natriuretic action.