Amphiphilic Cationic beta(3R3)-Peptides: Membrane Active Peptidomimetics and Their Potential as Antimicrobial Agents

作者：Mosca Simone; Keller Janos; Azzouz Nahid; Wagner Stefanie; Titz Alexander; Seeberger Peter H; Brezesinski Gerald; Hartmann Laura^*

来源：Biomacromolecules, 2014, 15(5): 1687-1695.

DOI：10.1021/bm500101w

We introduce a novel class of membrane active peptidomimetics, the amphiphilic cationic beta(3R3)-peptides, and evaluate their potential as antimicrobial agents. The design criteria, the building block and oligomer synthesis as well as a detailed structure-activity relationship (SAR) study are reported. Specifically, infrared reflection absorption spectroscopy (IRRAS) was employed to investigate structural features of amphiphilic cationic beta(3R3)-peptide sequences at the hydrophobic/hydrophilic air/liquid interface. Furthermore, Langmuir monolayers of anionic and zwitterionic phospholipids have been used to model the interactions of amphiphilic cationic beta(3R3)-peptides with prokaryotic and eukaryotic cellular membranes in order to predict their membrane selectivity and elucidate their mechanism of action. Lastly, antimicrobial activity was tested against Gram-positive M. luteus and S. aureus as well as against Gram-negative E. coli and P. aeruginosa bacteria along with testing hemolytic activity and cytotoxicity. We found that amphiphilic cationic beta(3R3)-peptide sequences combine high and selective antimicrobial activity with exceptionally low cytotoxicity in comparison to values reported in the literature. Overall, this study provides further insights into the SAR of antimicrobial peptides and peptidomimetics and indicates that amphiphilic cationic beta(3R3)-peptides are strong candidates for further development as antimicrobial agents with high therapeutic index.

• 出版日期2014-5