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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...

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Autores principales: Marracino, Paolo, Bernardi, Mario, Liberti, Micaela, Del Signore, Federico, Trapani, Erika, Gárate, José-Antonio, Burnham, Christian J., Apollonio, Francesca, English, Niall J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
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.
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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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