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Title
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Synergistic effect of electric field and lipid oxidation on the permeability of cell membranes
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Author
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Abstract
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| Background: Strong electric fields are known to affect cell membrane permeability, which can be applied for therapeutic purposes, e.g., in cancer therapy. A synergistic enhancement of this effect may be accomplished by the presence of reactive oxygen species (ROS), as generated in cold atmospheric plasmas. Little is known about the synergy between lipid oxidation by ROS and the electric field, nor on how this affects the cell membrane permeability. Method: We here conduct molecular dynamics simulations to elucidate the dynamics of the permeation process under the influence of combined lipid oxidation and electroporation. A phospholipid bilayer (PLB), consisting of di-oleoyl-phosphatidylcholine molecules covered with water layers, is used as a model system for the plasma membrane. Results and conclusions: We show how oxidation of the lipids in the PLB leads to an increase of the permeability of the bilayer to ROS, although the permeation free energy barriers still remain relatively high. More importantly, oxidation of the lipids results in a drop of the electric field threshold needed for pore formation (i.e., electroporation) in the PLB. The created pores in the membrane facilitate the penetration of reactive plasma species deep into the cell interior, eventually causing oxidative damage. General significance: This study is of particular interest for plasma medicine, as plasma generates both ROS and electric fields, but it is also of more general interest for applications where strong electric fields and ROS both come into play.(C) 2017 Elsevier B.V. All rights reserved. |
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Language
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English
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Source (journal)
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Biochimica et biophysica acta : G : general subjects. - Amsterdam, 1964, currens
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Publication
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Amsterdam
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Elsevier
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2017
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ISSN
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0304-4165
[print]
1872-8006
[online]
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DOI
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10.1016/J.BBAGEN.2017.01.030
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Volume/pages
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1861
:4
(2017)
, p. 839-847
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ISI
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000397366200012
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Pubmed ID
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28137619
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Full text (Publisher's DOI)
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Full text (open access)
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Full text (publisher's version - intranet only)
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