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Optoregulated force application to cellular receptors using molecular motors
Progress in our understanding of mechanotransduction events requires noninvasive methods for the manipulation of forces at molecular scale in physiological environments. Inspired by cellular mechanisms for force application (i.e. motor proteins pulling on cytoskeletal fibers), we present a unique mo...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8196032/ https://www.ncbi.nlm.nih.gov/pubmed/34117256 http://dx.doi.org/10.1038/s41467-021-23815-4 |
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author | Zheng, Yijun Han, Mitchell K. L. Zhao, Renping Blass, Johanna Zhang, Jingnan Zhou, Dennis W. Colard-Itté, Jean-Rémy Dattler, Damien Çolak, Arzu Hoth, Markus García, Andrés J. Qu, Bin Bennewitz, Roland Giuseppone, Nicolas del Campo, Aránzazu |
author_facet | Zheng, Yijun Han, Mitchell K. L. Zhao, Renping Blass, Johanna Zhang, Jingnan Zhou, Dennis W. Colard-Itté, Jean-Rémy Dattler, Damien Çolak, Arzu Hoth, Markus García, Andrés J. Qu, Bin Bennewitz, Roland Giuseppone, Nicolas del Campo, Aránzazu |
author_sort | Zheng, Yijun |
collection | PubMed |
description | Progress in our understanding of mechanotransduction events requires noninvasive methods for the manipulation of forces at molecular scale in physiological environments. Inspired by cellular mechanisms for force application (i.e. motor proteins pulling on cytoskeletal fibers), we present a unique molecular machine that can apply forces at cell-matrix and cell-cell junctions using light as an energy source. The key actuator is a light-driven rotatory molecular motor linked to polymer chains, which is intercalated between a membrane receptor and an engineered biointerface. The light-driven actuation of the molecular motor is converted in mechanical twisting of the entangled polymer chains, which will in turn effectively “pull” on engaged cell membrane receptors (e.g., integrins, T cell receptors) within the illuminated area. Applied forces have physiologically-relevant magnitude and occur at time scales within the relevant ranges for mechanotransduction at cell-friendly exposure conditions, as demonstrated in force-dependent focal adhesion maturation and T cell activation experiments. Our results reveal the potential of nanomotors for the manipulation of living cells at the molecular scale and demonstrate a functionality which at the moment cannot be achieved by other technologies for force application. |
format | Online Article Text |
id | pubmed-8196032 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81960322021-07-01 Optoregulated force application to cellular receptors using molecular motors Zheng, Yijun Han, Mitchell K. L. Zhao, Renping Blass, Johanna Zhang, Jingnan Zhou, Dennis W. Colard-Itté, Jean-Rémy Dattler, Damien Çolak, Arzu Hoth, Markus García, Andrés J. Qu, Bin Bennewitz, Roland Giuseppone, Nicolas del Campo, Aránzazu Nat Commun Article Progress in our understanding of mechanotransduction events requires noninvasive methods for the manipulation of forces at molecular scale in physiological environments. Inspired by cellular mechanisms for force application (i.e. motor proteins pulling on cytoskeletal fibers), we present a unique molecular machine that can apply forces at cell-matrix and cell-cell junctions using light as an energy source. The key actuator is a light-driven rotatory molecular motor linked to polymer chains, which is intercalated between a membrane receptor and an engineered biointerface. The light-driven actuation of the molecular motor is converted in mechanical twisting of the entangled polymer chains, which will in turn effectively “pull” on engaged cell membrane receptors (e.g., integrins, T cell receptors) within the illuminated area. Applied forces have physiologically-relevant magnitude and occur at time scales within the relevant ranges for mechanotransduction at cell-friendly exposure conditions, as demonstrated in force-dependent focal adhesion maturation and T cell activation experiments. Our results reveal the potential of nanomotors for the manipulation of living cells at the molecular scale and demonstrate a functionality which at the moment cannot be achieved by other technologies for force application. Nature Publishing Group UK 2021-06-11 /pmc/articles/PMC8196032/ /pubmed/34117256 http://dx.doi.org/10.1038/s41467-021-23815-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Zheng, Yijun Han, Mitchell K. L. Zhao, Renping Blass, Johanna Zhang, Jingnan Zhou, Dennis W. Colard-Itté, Jean-Rémy Dattler, Damien Çolak, Arzu Hoth, Markus García, Andrés J. Qu, Bin Bennewitz, Roland Giuseppone, Nicolas del Campo, Aránzazu Optoregulated force application to cellular receptors using molecular motors |
title | Optoregulated force application to cellular receptors using molecular motors |
title_full | Optoregulated force application to cellular receptors using molecular motors |
title_fullStr | Optoregulated force application to cellular receptors using molecular motors |
title_full_unstemmed | Optoregulated force application to cellular receptors using molecular motors |
title_short | Optoregulated force application to cellular receptors using molecular motors |
title_sort | optoregulated force application to cellular receptors using molecular motors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8196032/ https://www.ncbi.nlm.nih.gov/pubmed/34117256 http://dx.doi.org/10.1038/s41467-021-23815-4 |
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