# Electric field-induced rupture kinetics of giant unilamellar vesicles with varying gramicidin A content in membrane

## TL;DR

This study shows how gramicidin A affects the rupture of cell-like membranes under electric fields, with low amounts increasing stability and high amounts causing faster rupture.

## Contribution

The study reveals a non-monotonic effect of gramicidin A on membrane rupture kinetics under electric fields, providing new insights into lipid membrane electromechanical properties.

## Key findings

- Low gramicidin A content (0–0.05 mole%) increases membrane stability and reduces rupture probability.
- High gramicidin A content (0.05–5%) accelerates rupture kinetics and decreases membrane integrity.
- Pore-edge tension reaches a minimum at intermediate gramicidin A levels (0.05%), consistent with a theoretical electroporation model.

## Abstract

In this study, we examine the rupture kinetics of giant unilamellar vesicles (GUVs) composed of DOPG/DOPC and varying mole fractions of gramicidin A (GrA), under externally applied electric fields. Time-resolved fluorescence microscopy reveals that the presence of GrA modulates vesicle rupture behavior in a non-monotonic fashion. At lower contents of GrA (0–0.05 mole%), GUVs exhibit enhanced structural resilience, with significantly reduced rupture probability, suggesting increased membrane stability. However, at higher contents of GrA (0.05–5%), vesicles display accelerated rupture kinetics, reflecting decreased membrane integrity. Quantitative analysis of rupture events indicates a biphasic dependence of the rupture rate constant on GrA content. The pore-edge tension was obtained from the slope of the fitted linear relation between the logarithm of the rupture rate constant and the inverse of effective membrane tension for different GrA%. The pore-edge tension varies nonlinearly with GrA%, reaching a minimum at intermediate GrA levels (0.05%). These findings are consistent with a theoretical model for electroporation, where pore formation is governed by a balance between destabilizing electric tension and stabilizing line tension. The results highlight how lower mole% of GrA enhance membrane mechanical robustness, while excessive GrA incorporation disrupts bilayer cohesion and accelerates electroporation. This study provides new insights into the tunable electromechanical properties of lipid membranes modulated by membrane-active peptides.