Dual action of BPC194: a membrane active peptide killing bacterial cells.

Abstract

Membrane active peptides can perturb the lipid bilayer in several ways, such as poration and fusion of the target cell membrane, and thereby efficiently kill bacterial cells. We probe here the mechanistic basis of membrane poration and fusion caused by membrane-active, antimicrobial peptides. We show that the cyclic antimicrobial peptide, BPC194, inhibits growth of Gram-negative bacteria and ruptures the outer and inner membrane at the onset of killing, suggesting that not just poration is taking place at the cell envelope. To simplify the system and to better understand the mechanism of action, we performed Förster resonance energy transfer and cryogenic transmission electron microscopy studies in model membranes and show that the BPC194 causes fusion of vesicles. The fusogenic action is accompanied by leakage as probed by dual-color fluorescence burst analysis at a single liposome level. Atomistic molecular dynamics simulations reveal how the peptides are able to simultaneously perturb the membrane towards porated and fused states. We show that the cyclic antimicrobial peptides trigger both fusion and pore formation and that such large membrane perturbations have a similar mechanistic basis.

• Authors: Gemma Moiset, Anna D Cirac, Marc C A Stuart, Siewert-Jan Marrink, Durba Sengupta, Bert Poolman
• Journal: PloS one (PLoS One) Vol. 8 Issue 4 Pg. e61541 ( 2013) ISSN: 1932-6203 [Electronic] United States
• PMID: 23620763 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Antimicrobial Cationic Peptides
• BPC194
• Peptides, Cyclic

Topics

• Antimicrobial Cationic Peptides (pharmacology)
• Cell Membrane (drug effects, ultrastructure)
• Cell Proliferation (drug effects)
• Escherichia coli (cytology, drug effects, ultrastructure)
• Membrane Fusion (drug effects)
• Microbial Sensitivity Tests
• Microbial Viability (drug effects)
• Molecular Dynamics Simulation
• Peptides, Cyclic (pharmacology)