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Updated: Jul 1, 2025

Automated Lipid Bilayer Membrane Formation Using a Polydimethylsiloxane Thin Film
Published on: July 10, 2016
Effect of Phosphatidylethanolamine on Pore Formation Induced by the Antimicrobial Peptide PGLa
Marzuk Ahmed1, Md Zahidul Islam2, Md Masum Billah1
1Integrated Bioscience Section, Graduate School of Science and Technology, Shizuoka University, Shizuoka 422-8529, Japan.
Abstract:
Most antimicrobial peptides (AMPs) induce pore formation and a burst of lipid bilayers and plasma membranes. This causes severe leakage of the internal contents and cell death. The AMP PGLa forms nanopores in giant unilamellar vesicles (GUVs) comprising dioleoylphosphatidylcholine (DOPC) and dioleoylphosphatidylglycerol (DOPG). We here elucidated the effect of the line tension of a prepore rim on PGLa-induced nanopore formation by investigating the interaction of PGLa with single GUVs comprising dioleoylphosphatidylethanolamine (DOPE)/DOPG (6:4) in buffer using the single GUV method. We found that PGLa forms nanopores in the GUV membrane, which evolved into a local burst and burst of GUVs. The rate of pore formation in DOPE/DOPG-GUVs was smaller than that in DOPC/DOPG-GUVs. PGLa is located only in the outer leaflet of a GUV bilayer just before a fluorescent probe AF647 leakage from the inside, indicating that this asymmetric distribution induces nanopore formation. PGLa-induced local burst and burst of GUVs were observed at 10 ms-time resolution. After nanopore formation started, dense particles and small vesicles appeared in the GUVs, followed by a decrease in the GUV diameter. The GUV was finally converted into smaller GUV or lipid membrane aggregates. We discuss the mechanisms of PGLa-induced nanopore formation and its direct evolution to a GUV burst.
Insights
Antimicrobial peptide PGLa forms nanopores in lipid membranes, leading to cell death. This study reveals how PGLa
Area of Science:
- Biophysics
- Membrane Biology
- Antimicrobial Peptides
Background:
- Antimicrobial peptides (AMPs) are crucial for innate immunity.
- AMPs like PGLa induce cell death by forming pores in lipid bilayers.
- Understanding PGLa's mechanism is key to developing new antimicrobial strategies.
Purpose of the Study:
- To elucidate the effect of line tension on PGLa-induced nanopore formation.
- To investigate the interaction of PGLa with single giant unilamellar vesicles (GUVs).
- To understand the dynamics of PGLa-induced GUV membrane rupture.
Main Methods:
- Single GUV assay with time-resolved imaging (10 ms resolution).
- Utilized GUVs composed of dioleoylphosphatidylethanolamine (DOPE)/dioleoylphosphatidylglycerol (DOPG).
- Monitored PGLa interaction and subsequent membrane events via fluorescence leakage.
Main Results:
- PGLa induced nanopore formation and subsequent GUV burst in DOPE/DOPG GUVs.
- Pore formation rate was lower in DOPE/DOPG GUVs compared to DOPC/DOPG GUVs.
- Asymmetric distribution of PGLa in the outer leaflet preceded pore formation and leakage.
Conclusions:
- PGLa initiates nanopore formation through asymmetric membrane insertion.
- Nanopore formation rapidly evolves into GUV rupture and disintegration.
- Line tension plays a role in PGLa-mediated membrane destabilization and cell lysis.
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