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Competing instabilities reveal how to rationally design and control active crosslinked gels

How active stresses generated by molecular motors set the large-scale mechanics of the cell cytoskeleton remains poorly understood. Here, we combine experiments and theory to demonstrate how the emergent properties of a biomimetic active crosslinked gel depend on the properties of its microscopic co...

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Autores principales: Najma, Bibi, Varghese, Minu, Tsidilkovski, Lev, Lemma, Linnea, Baskaran, Aparna, Duclos, Guillaume
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9617906/
https://www.ncbi.nlm.nih.gov/pubmed/36309493
http://dx.doi.org/10.1038/s41467-022-34089-9
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author Najma, Bibi
Varghese, Minu
Tsidilkovski, Lev
Lemma, Linnea
Baskaran, Aparna
Duclos, Guillaume
author_facet Najma, Bibi
Varghese, Minu
Tsidilkovski, Lev
Lemma, Linnea
Baskaran, Aparna
Duclos, Guillaume
author_sort Najma, Bibi
collection PubMed
description How active stresses generated by molecular motors set the large-scale mechanics of the cell cytoskeleton remains poorly understood. Here, we combine experiments and theory to demonstrate how the emergent properties of a biomimetic active crosslinked gel depend on the properties of its microscopic constituents. We show that an extensile nematic elastomer exhibits two distinct activity-driven instabilities, spontaneously bending in-plane or buckling out-of-plane depending on its composition. Molecular motors play a dual antagonistic role, fluidizing or stiffening the gel depending on the ATP concentration. We demonstrate how active and elastic stresses are set by each component, providing estimates for the active gel theory parameters. Finally, activity and elasticity were manipulated in situ with light-activable motor proteins, controlling the direction of the instability optically. These results highlight how cytoskeletal stresses regulate the self-organization of living matter and set the foundations for the rational design and optogenetic control of active materials.
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spelling pubmed-96179062022-10-31 Competing instabilities reveal how to rationally design and control active crosslinked gels Najma, Bibi Varghese, Minu Tsidilkovski, Lev Lemma, Linnea Baskaran, Aparna Duclos, Guillaume Nat Commun Article How active stresses generated by molecular motors set the large-scale mechanics of the cell cytoskeleton remains poorly understood. Here, we combine experiments and theory to demonstrate how the emergent properties of a biomimetic active crosslinked gel depend on the properties of its microscopic constituents. We show that an extensile nematic elastomer exhibits two distinct activity-driven instabilities, spontaneously bending in-plane or buckling out-of-plane depending on its composition. Molecular motors play a dual antagonistic role, fluidizing or stiffening the gel depending on the ATP concentration. We demonstrate how active and elastic stresses are set by each component, providing estimates for the active gel theory parameters. Finally, activity and elasticity were manipulated in situ with light-activable motor proteins, controlling the direction of the instability optically. These results highlight how cytoskeletal stresses regulate the self-organization of living matter and set the foundations for the rational design and optogenetic control of active materials. Nature Publishing Group UK 2022-10-29 /pmc/articles/PMC9617906/ /pubmed/36309493 http://dx.doi.org/10.1038/s41467-022-34089-9 Text en © The Author(s) 2022 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
Najma, Bibi
Varghese, Minu
Tsidilkovski, Lev
Lemma, Linnea
Baskaran, Aparna
Duclos, Guillaume
Competing instabilities reveal how to rationally design and control active crosslinked gels
title Competing instabilities reveal how to rationally design and control active crosslinked gels
title_full Competing instabilities reveal how to rationally design and control active crosslinked gels
title_fullStr Competing instabilities reveal how to rationally design and control active crosslinked gels
title_full_unstemmed Competing instabilities reveal how to rationally design and control active crosslinked gels
title_short Competing instabilities reveal how to rationally design and control active crosslinked gels
title_sort competing instabilities reveal how to rationally design and control active crosslinked gels
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9617906/
https://www.ncbi.nlm.nih.gov/pubmed/36309493
http://dx.doi.org/10.1038/s41467-022-34089-9
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