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Varying crosslinking motifs drive the mesoscale mechanics of actin-microtubule composites
The cytoskeleton precisely tunes its mechanics by altering interactions between semiflexible actin filaments, rigid microtubules, and crosslinking proteins. We use optical tweezers microrheology and confocal microscopy to characterize how varying crosslinking motifs impact the mesoscale mechanics an...
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/PMC6731314/ https://www.ncbi.nlm.nih.gov/pubmed/31492892 http://dx.doi.org/10.1038/s41598-019-49236-4 |
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author | Ricketts, Shea N. Francis, Madison L. Farhadi, Leila Rust, Michael J. Das, Moumita Ross, Jennifer L. Robertson-Anderson, Rae M. |
author_facet | Ricketts, Shea N. Francis, Madison L. Farhadi, Leila Rust, Michael J. Das, Moumita Ross, Jennifer L. Robertson-Anderson, Rae M. |
author_sort | Ricketts, Shea N. |
collection | PubMed |
description | The cytoskeleton precisely tunes its mechanics by altering interactions between semiflexible actin filaments, rigid microtubules, and crosslinking proteins. We use optical tweezers microrheology and confocal microscopy to characterize how varying crosslinking motifs impact the mesoscale mechanics and mobility of actin-microtubule composites. We show that, upon subtle changes in crosslinking patterns, composites can exhibit two distinct classes of force response – primarily elastic versus more viscous. For example, a composite in which actin and microtubules are crosslinked to each other but not to themselves is markedly more elastic than one in which both filaments are independently crosslinked. Notably, this distinction only emerges at mesoscopic scales in response to nonlinear forcing, whereas varying crosslinking motifs have little impact on the microscale mechanics and mobility. Our unexpected scale-dependent results not only inform the physics underlying key cytoskeleton processes and structures, but, more generally, provide valuable perspective to materials engineering endeavors focused on polymer composites. |
format | Online Article Text |
id | pubmed-6731314 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67313142019-09-18 Varying crosslinking motifs drive the mesoscale mechanics of actin-microtubule composites Ricketts, Shea N. Francis, Madison L. Farhadi, Leila Rust, Michael J. Das, Moumita Ross, Jennifer L. Robertson-Anderson, Rae M. Sci Rep Article The cytoskeleton precisely tunes its mechanics by altering interactions between semiflexible actin filaments, rigid microtubules, and crosslinking proteins. We use optical tweezers microrheology and confocal microscopy to characterize how varying crosslinking motifs impact the mesoscale mechanics and mobility of actin-microtubule composites. We show that, upon subtle changes in crosslinking patterns, composites can exhibit two distinct classes of force response – primarily elastic versus more viscous. For example, a composite in which actin and microtubules are crosslinked to each other but not to themselves is markedly more elastic than one in which both filaments are independently crosslinked. Notably, this distinction only emerges at mesoscopic scales in response to nonlinear forcing, whereas varying crosslinking motifs have little impact on the microscale mechanics and mobility. Our unexpected scale-dependent results not only inform the physics underlying key cytoskeleton processes and structures, but, more generally, provide valuable perspective to materials engineering endeavors focused on polymer composites. Nature Publishing Group UK 2019-09-06 /pmc/articles/PMC6731314/ /pubmed/31492892 http://dx.doi.org/10.1038/s41598-019-49236-4 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 Ricketts, Shea N. Francis, Madison L. Farhadi, Leila Rust, Michael J. Das, Moumita Ross, Jennifer L. Robertson-Anderson, Rae M. Varying crosslinking motifs drive the mesoscale mechanics of actin-microtubule composites |
title | Varying crosslinking motifs drive the mesoscale mechanics of actin-microtubule composites |
title_full | Varying crosslinking motifs drive the mesoscale mechanics of actin-microtubule composites |
title_fullStr | Varying crosslinking motifs drive the mesoscale mechanics of actin-microtubule composites |
title_full_unstemmed | Varying crosslinking motifs drive the mesoscale mechanics of actin-microtubule composites |
title_short | Varying crosslinking motifs drive the mesoscale mechanics of actin-microtubule composites |
title_sort | varying crosslinking motifs drive the mesoscale mechanics of actin-microtubule composites |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6731314/ https://www.ncbi.nlm.nih.gov/pubmed/31492892 http://dx.doi.org/10.1038/s41598-019-49236-4 |
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