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March 21, 2026ChemBioChem0 citationsOpen Access

Instant Membrane Stabilization by Damage‐Triggered Actin Polymerization in Giant Unilamellar Vesicles

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HNHuong Thanh NguyenSLSang Ho LeeCKChang Ho Kim

Key Points

  • To investigate a damage-triggered mechanism for stabilizing membranes in giant unilamellar vesicles (GUVs).
  • Encapsulated ATP-activated G-actin in divalent-cation-free lumen of GUVs.
  • Supplied high concentrations of Ca2+ or Mg2+ externally to induce cation influx.
  • Induced F-actin assembly upon membrane poration to create a mechanical meshwork.
  • Localized cation entry led to rapid assembly of F-actin at membrane defects.
  • F-actin formation prevented further pore enlargement and preserved vesicle morphology.
  • Actin plug improved vesicle survival against rupture, although full impermeability was not restored.

Abstract

Giant unilamellar vesicles (GUVs) rupture catastrophically when membrane pores expand under tension, because they lack cellular repair machinery. Here we present a minimal, damage-triggered stabilization mechanism based on rapid actin polymerization inside GUVs. ATP-activated G-actin was encapsulated in a divalent-cation-free lumen while high concentrations of Ca2+ or Mg2+ were supplied externally, creating a condition where membrane poration immediately drives cation influx. Upon poration, localized cation entry induces fast F-actin assembly that forms a cortical-like meshwork at the defect, mechanically arresting pore enlargement and preserving vesicle morphology for extended periods. The resulting actin plug does not restore full impermeability to small molecules, but it substantially increases vesicle survival against rupture and recapitulates the "plugging" aspect of single-cell membrane wound responses in a bottom-up artificial cell model.

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Cite This Study

Nguyen et al. (2026) studied this question.

synapsesocial.com/papers/69be35d76e48c4981c6743f8https://doi.org/10.1002/cbic.202500974
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