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Transprotein-Electropore Characterization: A Molecular Dynamics Investigation on Human AQP4
[Image: see text] Electroporation characterization is a topic of intensive interest probed by extensive ongoing research efforts. Usually, these studies are carried out on lipid-bilayer electroporation. Surprisingly, the possibility of water-channel electropore formation across transmembrane protein...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288775/ https://www.ncbi.nlm.nih.gov/pubmed/30556005 http://dx.doi.org/10.1021/acsomega.8b02230 |
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author | Marracino, Paolo Bernardi, Mario Liberti, Micaela Del Signore, Federico Trapani, Erika Gárate, José-Antonio Burnham, Christian J. Apollonio, Francesca English, Niall J. |
author_facet | Marracino, Paolo Bernardi, Mario Liberti, Micaela Del Signore, Federico Trapani, Erika Gárate, José-Antonio Burnham, Christian J. Apollonio, Francesca English, Niall J. |
author_sort | Marracino, Paolo |
collection | PubMed |
description | [Image: see text] Electroporation characterization is a topic of intensive interest probed by extensive ongoing research efforts. Usually, these studies are carried out on lipid-bilayer electroporation. Surprisingly, the possibility of water-channel electropore formation across transmembrane proteins themselves, particularly in view of such a promising application, has not yet been elucidated. The present work examines the geometrical and kinetic aspects of electropores and their stability in such a protein milieux (as opposed through the phospholipid membranes) in depth, by means of scrutiny of such a process in human-AQP4 as a well-representative prototype. The residues forming the electropore’s walls, organized in loops, reveal the formation mechanism by their dipole alignment and translational response in response to applied axial electric fields in nonequilibrium molecular dynamics simulation. The magnitude of sustaining electric fields (keeping a stable electropore open) were determined. This suggests that transmembrane proteins could play a central role in electroporation applications, e.g., in medicine and biotechnology. |
format | Online Article Text |
id | pubmed-6288775 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-62887752018-12-12 Transprotein-Electropore Characterization: A Molecular Dynamics Investigation on Human AQP4 Marracino, Paolo Bernardi, Mario Liberti, Micaela Del Signore, Federico Trapani, Erika Gárate, José-Antonio Burnham, Christian J. Apollonio, Francesca English, Niall J. ACS Omega [Image: see text] Electroporation characterization is a topic of intensive interest probed by extensive ongoing research efforts. Usually, these studies are carried out on lipid-bilayer electroporation. Surprisingly, the possibility of water-channel electropore formation across transmembrane proteins themselves, particularly in view of such a promising application, has not yet been elucidated. The present work examines the geometrical and kinetic aspects of electropores and their stability in such a protein milieux (as opposed through the phospholipid membranes) in depth, by means of scrutiny of such a process in human-AQP4 as a well-representative prototype. The residues forming the electropore’s walls, organized in loops, reveal the formation mechanism by their dipole alignment and translational response in response to applied axial electric fields in nonequilibrium molecular dynamics simulation. The magnitude of sustaining electric fields (keeping a stable electropore open) were determined. This suggests that transmembrane proteins could play a central role in electroporation applications, e.g., in medicine and biotechnology. American Chemical Society 2018-11-13 /pmc/articles/PMC6288775/ /pubmed/30556005 http://dx.doi.org/10.1021/acsomega.8b02230 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Marracino, Paolo Bernardi, Mario Liberti, Micaela Del Signore, Federico Trapani, Erika Gárate, José-Antonio Burnham, Christian J. Apollonio, Francesca English, Niall J. Transprotein-Electropore Characterization: A Molecular Dynamics Investigation on Human AQP4 |
title | Transprotein-Electropore Characterization: A Molecular
Dynamics Investigation on Human AQP4 |
title_full | Transprotein-Electropore Characterization: A Molecular
Dynamics Investigation on Human AQP4 |
title_fullStr | Transprotein-Electropore Characterization: A Molecular
Dynamics Investigation on Human AQP4 |
title_full_unstemmed | Transprotein-Electropore Characterization: A Molecular
Dynamics Investigation on Human AQP4 |
title_short | Transprotein-Electropore Characterization: A Molecular
Dynamics Investigation on Human AQP4 |
title_sort | transprotein-electropore characterization: a molecular
dynamics investigation on human aqp4 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288775/ https://www.ncbi.nlm.nih.gov/pubmed/30556005 http://dx.doi.org/10.1021/acsomega.8b02230 |
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