Abstract
A large increase in the transmembrane voltage, U(t), of a fluid bilayer membrane is believed to result in the occurrence of temporary aqueous pathways ("pores") across the membrane. The number, size, and evolution dynamics of these pores are expected to be crucial to the transport of water-soluble species ranging from small ions to macromolecules such as proteins and nucleic acids. In this paper we use a transient aqueous pore theory to estimate the fraction of the membrane area, Fw(t), which is temporarily occupied by water-filled pores for short square, exponential, and bipolar square pulses. For short pulses, "reversible electrical breakdown" occurs when the transmembrane voltage reaches about 1 V, and Fw(t) is predicted to rise rapidly, but always to be less than 10(-3). The conductance of a large number of pores causes reversible electrical breakdown and prevents a significantly larger U from being reached. Despite the large dielectric constant of water, for reversible electroporation the associated change in membrane capacitance, delta C, due to the pores is predicted to be small. Moreover, for a flat membrane the minimum value of the mean pore-pore separation is large, about 60 times the minimum pore radius. In flat membranes, pores are predicted to repel, but the opposite is expected for curved cell membranes, allowing the possibility of coalescence in cell membranes. For some moderate values of U, rupture (irreversible electrical breakdown) occurs, as one or more supracritical pores expand to the membrane boundary and the entire membrane area becomes aqueous. In all cases it is found that a quantitative description of electroporation requires that a pore size distribution, rather than a single size pore.
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- Alvarez O., Latorre R. Voltage-dependent capacitance in lipid bilayers made from monolayers. Biophys J. 1978 Jan;21(1):1–17. doi: 10.1016/S0006-3495(78)85505-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bach D., Miller I. R. Glyceryl monooleate black lipid membranes obtained from squalene solutions. Biophys J. 1980 Jan;29(1):183–187. doi: 10.1016/S0006-3495(80)85125-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Benz R., Beckers F., Zimmermann U. Reversible electrical breakdown of lipid bilayer membranes: a charge-pulse relaxation study. J Membr Biol. 1979 Jul 16;48(2):181–204. doi: 10.1007/BF01872858. [DOI] [PubMed] [Google Scholar]
- Giles A. E., Lockyer C. Ovarian Pregnancy. Proc R Soc Med. 1915;8(OBSTET):2–10. doi: 10.1177/003591571500800902. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Glaser R. W., Leikin S. L., Chernomordik L. V., Pastushenko V. F., Sokirko A. I. Reversible electrical breakdown of lipid bilayers: formation and evolution of pores. Biochim Biophys Acta. 1988 May 24;940(2):275–287. doi: 10.1016/0005-2736(88)90202-7. [DOI] [PubMed] [Google Scholar]
- Hibino M., Shigemori M., Itoh H., Nagayama K., Kinosita K., Jr Membrane conductance of an electroporated cell analyzed by submicrosecond imaging of transmembrane potential. Biophys J. 1991 Jan;59(1):209–220. doi: 10.1016/S0006-3495(91)82212-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lipowsky R. The conformation of membranes. Nature. 1991 Feb 7;349(6309):475–481. doi: 10.1038/349475a0. [DOI] [PubMed] [Google Scholar]
- Orlowski S., Mir L. M. Cell electropermeabilization: a new tool for biochemical and pharmacological studies. Biochim Biophys Acta. 1993 Jun 8;1154(1):51–63. doi: 10.1016/0304-4157(93)90016-h. [DOI] [PubMed] [Google Scholar]
- Sugar I. P., Förster W., Neumann E. Model of cell electrofusion. Membrane electroporation, pore coalescence and percolation. Biophys Chem. 1987 May 9;26(2-3):321–335. doi: 10.1016/0301-4622(87)80033-9. [DOI] [PubMed] [Google Scholar]
- Sugar I. P., Neumann E. Stochastic model for electric field-induced membrane pores. Electroporation. Biophys Chem. 1984 May;19(3):211–225. doi: 10.1016/0301-4622(84)87003-9. [DOI] [PubMed] [Google Scholar]
- Sugár I. P. The effects of external fields on the structure of lipid bilayers. J Physiol (Paris) 1981 May;77(9):1035–1042. [PubMed] [Google Scholar]
- Toyama S., Nakamura A., Toda F. Measurement of voltage dependence of capacitance of planar bilayer lipid membrane with a patch clamp amplifier. Biophys J. 1991 Apr;59(4):939–944. doi: 10.1016/S0006-3495(91)82308-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tsong T. Y. Electroporation of cell membranes. Biophys J. 1991 Aug;60(2):297–306. doi: 10.1016/S0006-3495(91)82054-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Weaver J. C. Electroporation: a general phenomenon for manipulating cells and tissues. J Cell Biochem. 1993 Apr;51(4):426–435. doi: 10.1002/jcb.2400510407. [DOI] [PubMed] [Google Scholar]

