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Actin filaments function as a tension sensor by tension-dependent binding of cofilin to the filament

Intracellular and extracellular mechanical forces affect the structure and dynamics of the actin cytoskeleton. However, the underlying molecular and biophysical mechanisms, including how mechanical forces are sensed, are largely unknown. Actin-depolymerizing factor/cofilin proteins are actin-modulat...

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Detalles Bibliográficos
Autores principales: Hayakawa, Kimihide, Tatsumi, Hitoshi, Sokabe, Masahiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3257564/
https://www.ncbi.nlm.nih.gov/pubmed/22123860
http://dx.doi.org/10.1083/jcb.201102039
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author Hayakawa, Kimihide
Tatsumi, Hitoshi
Sokabe, Masahiro
author_facet Hayakawa, Kimihide
Tatsumi, Hitoshi
Sokabe, Masahiro
author_sort Hayakawa, Kimihide
collection PubMed
description Intracellular and extracellular mechanical forces affect the structure and dynamics of the actin cytoskeleton. However, the underlying molecular and biophysical mechanisms, including how mechanical forces are sensed, are largely unknown. Actin-depolymerizing factor/cofilin proteins are actin-modulating proteins that are ubiquitously distributed in eukaryotes, and they are the most likely candidate as proteins to drive stress fiber disassembly in response to changes in tension in the fiber. In this study, we propose a novel hypothesis that tension in an actin filament prevents the filament from being severed by cofilin. To test this, we placed single actin filaments under tension using optical tweezers. When a fiber was tensed, it was severed after the application of cofilin with a significantly larger delay in comparison with control filaments suspended in solution. The binding rate of cofilin to an actin bundle decreased when the bundle was tensed. These results suggest that tension in an actin filament reduces the cofilin binding, resulting in a decrease in its effective severing activity.
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spelling pubmed-32575642012-05-28 Actin filaments function as a tension sensor by tension-dependent binding of cofilin to the filament Hayakawa, Kimihide Tatsumi, Hitoshi Sokabe, Masahiro J Cell Biol Research Articles Intracellular and extracellular mechanical forces affect the structure and dynamics of the actin cytoskeleton. However, the underlying molecular and biophysical mechanisms, including how mechanical forces are sensed, are largely unknown. Actin-depolymerizing factor/cofilin proteins are actin-modulating proteins that are ubiquitously distributed in eukaryotes, and they are the most likely candidate as proteins to drive stress fiber disassembly in response to changes in tension in the fiber. In this study, we propose a novel hypothesis that tension in an actin filament prevents the filament from being severed by cofilin. To test this, we placed single actin filaments under tension using optical tweezers. When a fiber was tensed, it was severed after the application of cofilin with a significantly larger delay in comparison with control filaments suspended in solution. The binding rate of cofilin to an actin bundle decreased when the bundle was tensed. These results suggest that tension in an actin filament reduces the cofilin binding, resulting in a decrease in its effective severing activity. The Rockefeller University Press 2011-11-28 /pmc/articles/PMC3257564/ /pubmed/22123860 http://dx.doi.org/10.1083/jcb.201102039 Text en © 2011 Hayakawa et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Research Articles
Hayakawa, Kimihide
Tatsumi, Hitoshi
Sokabe, Masahiro
Actin filaments function as a tension sensor by tension-dependent binding of cofilin to the filament
title Actin filaments function as a tension sensor by tension-dependent binding of cofilin to the filament
title_full Actin filaments function as a tension sensor by tension-dependent binding of cofilin to the filament
title_fullStr Actin filaments function as a tension sensor by tension-dependent binding of cofilin to the filament
title_full_unstemmed Actin filaments function as a tension sensor by tension-dependent binding of cofilin to the filament
title_short Actin filaments function as a tension sensor by tension-dependent binding of cofilin to the filament
title_sort actin filaments function as a tension sensor by tension-dependent binding of cofilin to the filament
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3257564/
https://www.ncbi.nlm.nih.gov/pubmed/22123860
http://dx.doi.org/10.1083/jcb.201102039
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