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Molecular organization and mechanics of single vimentin filaments revealed by super-resolution imaging
Intermediate filaments (IFs) are involved in key cellular functions including polarization, migration, and protection against large deformations. These functions are related to their remarkable ability to extend without breaking, a capacity that should be determined by the molecular organization of...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8880768/ https://www.ncbi.nlm.nih.gov/pubmed/35213220 http://dx.doi.org/10.1126/sciadv.abm2696 |
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author | Nunes Vicente, Filipe Lelek, Mickael Tinevez, Jean-Yves Tran, Quang D. Pehau-Arnaudet, Gerard Zimmer, Christophe Etienne-Manneville, Sandrine Giannone, Gregory Leduc, Cécile |
author_facet | Nunes Vicente, Filipe Lelek, Mickael Tinevez, Jean-Yves Tran, Quang D. Pehau-Arnaudet, Gerard Zimmer, Christophe Etienne-Manneville, Sandrine Giannone, Gregory Leduc, Cécile |
author_sort | Nunes Vicente, Filipe |
collection | PubMed |
description | Intermediate filaments (IFs) are involved in key cellular functions including polarization, migration, and protection against large deformations. These functions are related to their remarkable ability to extend without breaking, a capacity that should be determined by the molecular organization of subunits within filaments. However, this structure-mechanics relationship remains poorly understood at the molecular level. Here, using super-resolution microscopy (SRM), we show that vimentin filaments exhibit a ~49-nanometer axial repeat both in cells and in vitro. As unit-length filaments (ULFs) were measured at ~59 nanometers, this demonstrates a partial overlap of ULFs during filament assembly. Using an SRM-compatible stretching device, we also provide evidence that the extensibility of vimentin is due to the unfolding of its subunits and not to their sliding, thus establishing a direct link between the structural organization and its mechanical properties. Overall, our results pave the way for future studies of IF assembly, mechanical, and structural properties in cells. |
format | Online Article Text |
id | pubmed-8880768 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-88807682022-03-10 Molecular organization and mechanics of single vimentin filaments revealed by super-resolution imaging Nunes Vicente, Filipe Lelek, Mickael Tinevez, Jean-Yves Tran, Quang D. Pehau-Arnaudet, Gerard Zimmer, Christophe Etienne-Manneville, Sandrine Giannone, Gregory Leduc, Cécile Sci Adv Biomedicine and Life Sciences Intermediate filaments (IFs) are involved in key cellular functions including polarization, migration, and protection against large deformations. These functions are related to their remarkable ability to extend without breaking, a capacity that should be determined by the molecular organization of subunits within filaments. However, this structure-mechanics relationship remains poorly understood at the molecular level. Here, using super-resolution microscopy (SRM), we show that vimentin filaments exhibit a ~49-nanometer axial repeat both in cells and in vitro. As unit-length filaments (ULFs) were measured at ~59 nanometers, this demonstrates a partial overlap of ULFs during filament assembly. Using an SRM-compatible stretching device, we also provide evidence that the extensibility of vimentin is due to the unfolding of its subunits and not to their sliding, thus establishing a direct link between the structural organization and its mechanical properties. Overall, our results pave the way for future studies of IF assembly, mechanical, and structural properties in cells. American Association for the Advancement of Science 2022-02-25 /pmc/articles/PMC8880768/ /pubmed/35213220 http://dx.doi.org/10.1126/sciadv.abm2696 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Nunes Vicente, Filipe Lelek, Mickael Tinevez, Jean-Yves Tran, Quang D. Pehau-Arnaudet, Gerard Zimmer, Christophe Etienne-Manneville, Sandrine Giannone, Gregory Leduc, Cécile Molecular organization and mechanics of single vimentin filaments revealed by super-resolution imaging |
title | Molecular organization and mechanics of single vimentin filaments revealed by super-resolution imaging |
title_full | Molecular organization and mechanics of single vimentin filaments revealed by super-resolution imaging |
title_fullStr | Molecular organization and mechanics of single vimentin filaments revealed by super-resolution imaging |
title_full_unstemmed | Molecular organization and mechanics of single vimentin filaments revealed by super-resolution imaging |
title_short | Molecular organization and mechanics of single vimentin filaments revealed by super-resolution imaging |
title_sort | molecular organization and mechanics of single vimentin filaments revealed by super-resolution imaging |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8880768/ https://www.ncbi.nlm.nih.gov/pubmed/35213220 http://dx.doi.org/10.1126/sciadv.abm2696 |
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