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Tubulin response to intense nanosecond-scale electric field in molecular dynamics simulation
Intense pulsed electric fields are known to act at the cell membrane level and are already being exploited in biomedical and biotechnological applications. However, it is not clear if electric pulses within biomedically-attainable parameters could directly influence intra-cellular components such as...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6642143/ https://www.ncbi.nlm.nih.gov/pubmed/31324834 http://dx.doi.org/10.1038/s41598-019-46636-4 |
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author | Marracino, Paolo Havelka, Daniel Průša, Jiří Liberti, Micaela Tuszynski, Jack Ayoub, Ahmed T. Apollonio, Francesca Cifra, Michal |
author_facet | Marracino, Paolo Havelka, Daniel Průša, Jiří Liberti, Micaela Tuszynski, Jack Ayoub, Ahmed T. Apollonio, Francesca Cifra, Michal |
author_sort | Marracino, Paolo |
collection | PubMed |
description | Intense pulsed electric fields are known to act at the cell membrane level and are already being exploited in biomedical and biotechnological applications. However, it is not clear if electric pulses within biomedically-attainable parameters could directly influence intra-cellular components such as cytoskeletal proteins. If so, a molecular mechanism of action could be uncovered for therapeutic applications of such electric fields. To help clarify this question, we first identified that a tubulin heterodimer is a natural biological target for intense electric fields due to its exceptional electric properties and crucial roles played in cell division. Using molecular dynamics simulations, we then demonstrated that an intense - yet experimentally attainable - electric field of nanosecond duration can affect the bβ-tubulin’s C-terminus conformations and also influence local electrostatic properties at the GTPase as well as the binding sites of major tubulin drugs site. Our results suggest that intense nanosecond electric pulses could be used for physical modulation of microtubule dynamics. Since a nanosecond pulsed electric field can penetrate the tissues and cellular membranes due to its broadband spectrum, our results are also potentially significant for the development of new therapeutic protocols. |
format | Online Article Text |
id | pubmed-6642143 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66421432019-07-25 Tubulin response to intense nanosecond-scale electric field in molecular dynamics simulation Marracino, Paolo Havelka, Daniel Průša, Jiří Liberti, Micaela Tuszynski, Jack Ayoub, Ahmed T. Apollonio, Francesca Cifra, Michal Sci Rep Article Intense pulsed electric fields are known to act at the cell membrane level and are already being exploited in biomedical and biotechnological applications. However, it is not clear if electric pulses within biomedically-attainable parameters could directly influence intra-cellular components such as cytoskeletal proteins. If so, a molecular mechanism of action could be uncovered for therapeutic applications of such electric fields. To help clarify this question, we first identified that a tubulin heterodimer is a natural biological target for intense electric fields due to its exceptional electric properties and crucial roles played in cell division. Using molecular dynamics simulations, we then demonstrated that an intense - yet experimentally attainable - electric field of nanosecond duration can affect the bβ-tubulin’s C-terminus conformations and also influence local electrostatic properties at the GTPase as well as the binding sites of major tubulin drugs site. Our results suggest that intense nanosecond electric pulses could be used for physical modulation of microtubule dynamics. Since a nanosecond pulsed electric field can penetrate the tissues and cellular membranes due to its broadband spectrum, our results are also potentially significant for the development of new therapeutic protocols. Nature Publishing Group UK 2019-07-19 /pmc/articles/PMC6642143/ /pubmed/31324834 http://dx.doi.org/10.1038/s41598-019-46636-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Marracino, Paolo Havelka, Daniel Průša, Jiří Liberti, Micaela Tuszynski, Jack Ayoub, Ahmed T. Apollonio, Francesca Cifra, Michal Tubulin response to intense nanosecond-scale electric field in molecular dynamics simulation |
title | Tubulin response to intense nanosecond-scale electric field in molecular dynamics simulation |
title_full | Tubulin response to intense nanosecond-scale electric field in molecular dynamics simulation |
title_fullStr | Tubulin response to intense nanosecond-scale electric field in molecular dynamics simulation |
title_full_unstemmed | Tubulin response to intense nanosecond-scale electric field in molecular dynamics simulation |
title_short | Tubulin response to intense nanosecond-scale electric field in molecular dynamics simulation |
title_sort | tubulin response to intense nanosecond-scale electric field in molecular dynamics simulation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6642143/ https://www.ncbi.nlm.nih.gov/pubmed/31324834 http://dx.doi.org/10.1038/s41598-019-46636-4 |
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