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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...

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Autores principales: Nunes Vicente, Filipe, Lelek, Mickael, Tinevez, Jean-Yves, Tran, Quang D., Pehau-Arnaudet, Gerard, Zimmer, Christophe, Etienne-Manneville, Sandrine, Giannone, Gregory, Leduc, Cécile
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2022
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.
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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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