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Originally published as Biophys J. BioFAST on December 13, 2004.
doi:10.1529/biophysj.104.050310
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Biophysical Journal 88:1143-1155 (2005)
© 2005 The Biophysical Society

Electro-Deformation and Poration of Giant Vesicles Viewed with High Temporal Resolution

Karin A. Riske and Rumiana Dimova

Max Planck Institute of Colloids and Interfaces, 14476 Golm, Germany

Correspondence: Address reprint requests to Dr. R. Dimova, Max Planck Institute of Colloids and Interfaces, Am Mühlenberg 1, 14476 Golm, Germany. Tel.: 49-331-567-9615; Fax: 49-331-567-9612; E-mail: dimova{at}mpikg.mpg.de.

Fast digital imaging was used to study the deformation and poration of giant unilamellar vesicles subjected to electric pulses. For the first time the dynamics of response and relaxation of the membrane at micron-scale level is revealed at a time resolution of 30 µs. Above a critical transmembrane potential the lipid bilayer ruptures. Formation of macropores (diameter ~2 µm) with pore lifetime of ~10 ms has been detected. The pore lifetime has been interpreted as interplay between the pore edge tension and the membrane viscosity. The reported data, covering six decades of time, show the following regimes in the relaxation dynamics of the membrane. Tensed vesicles first relax to release the acquired stress due to stretching, ~100 µs. In the case of poration, membrane resealing occurs with a characteristic time of ~10 ms. Finally, for vesicles with excess area an additional slow regime was observed, ~1 s, which we associate with relaxation of membrane curvature. Dimensional analysis can reasonably well explain the corresponding characteristic timescales. Being performed on cell-sized giant unilamellar vesicles, this study brings insight to cell electroporation. The latter is widely used for gene transfection and drug transport across the membrane where processes occurring at different timescales may influence the efficiency.




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