Fiche publication
Date publication
mars 2026
Journal
Biochimica et biophysica acta. Biomembranes
Auteurs
Membres identifiés du Cancéropôle Est :
Pr BECHINGER Burkhard
Tous les auteurs :
De K, Aisenbrey C, Hoernke M, Bechinger B
Lien Pubmed
Résumé
Antimicrobial peptides (AMPs) are hoped to complement classical antibiotics in view of increasing microbial resistance. We investigate two members of a family of designed cyclic AMPs with different activity and selectivity. The cyclic hexapeptides are rich in arginine and tryptophan and have been shown previously to target cell membranes and to affect model membranes differently depending on the lipid membrane composition. To better understand their mechanisms of membrane perturbation, we investigated the interactions of cyclic RRRWWW and cyclic RWRWRW with various model membranes containing lipids commonly found in either bacterial or eukaryotic membranes. Using P and H solid-state NMR methods, we systematically analyzed the interactions between the peptides and lipid membranes at the molecular level. When POPE/POPG model membranes are investigated the two peptides exhibit distinct interactions with the PE and PG components, reflected in a different decrease in lipid chain order parameters. This decrease in deuterium order parameters and deformation of the vesicle shapes indicate disturbance of the lipid membrane structure by the peptides. Our study provides new insights into the molecular mechanisms of AMP-membrane interactions and can contribute to the understanding and development of novel antimicrobial agents.
Mots clés
Antimicrobial cyclic peptides, Arginine-tryptophan rich peptides, lateral phase separation, Magnetic deformation, Order parameter, Peptide-lipid interaction
Référence
Biochim Biophys Acta Biomembr. 2026 03 5;:184519
