Calcium and phosphatidylserine inhibit lipid electropore formation and reduce pore lifetime
Journal of Membrane Biology, ISSN: 0022-2631, Vol: 245, Issue: 10, Page: 599-610
2012
- 39Citations
- 46Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations39
- Citation Indexes39
- 39
- CrossRef25
- Captures46
- Readers46
- 46
Article Description
Molecular dynamics simulations of electro-poration of homogeneous phospholipid bilayers show that the pore creation time is strongly dependent on the magnitude of the applied electric field. Here, we investigated whether heterogeneous bilayers containing phospholipids with zwitterionic and anionic headgroups exhibit a similar dependence. To facilitate this analysis we divide the life cycle of an electropore into several stages, marking the sequence of steps for pore creation and pore annihilation (restoration of the bilayer after removal of the electric field). We also report simulations of calcium binding isotherms and the effects of calcium ions on the electroporation of heterogeneous lipid bilayers. Calcium binding simulations are consistent with experimental data using a 1:2 Langmuir binding isotherm. We find that calcium ions and phosphatidylserine increase pore creation time and decrease pore annihilation time. For all systems tested, pore creation time was inversely proportional to the bilayer internal electric field. © Springer Science+Business Media, LLC 2012.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84867849495&origin=inward; http://dx.doi.org/10.1007/s00232-012-9471-1; http://www.ncbi.nlm.nih.gov/pubmed/22815071; http://link.springer.com/10.1007/s00232-012-9471-1; http://www.springerlink.com/index/10.1007/s00232-012-9471-1; http://www.springerlink.com/index/pdf/10.1007/s00232-012-9471-1; https://dx.doi.org/10.1007/s00232-012-9471-1; https://link.springer.com/article/10.1007/s00232-012-9471-1
Springer Science and Business Media LLC
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