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Phosphoinositides regulate force-independent interactions between talin, vinculin, and actin
Focal adhesions (FA) are large macromolecular assemblies which help transmit mechanical forces and regulatory signals between the extracellular matrix and an interacting cell. Two key proteins talin and vinculin connecting integrin to actomyosin networks in the cell. Both proteins bind to F-actin an...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7384861/ https://www.ncbi.nlm.nih.gov/pubmed/32657269 http://dx.doi.org/10.7554/eLife.56110 |
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author | Kelley, Charlotte F Litschel, Thomas Schumacher, Stephanie Dedden, Dirk Schwille, Petra Mizuno, Naoko |
author_facet | Kelley, Charlotte F Litschel, Thomas Schumacher, Stephanie Dedden, Dirk Schwille, Petra Mizuno, Naoko |
author_sort | Kelley, Charlotte F |
collection | PubMed |
description | Focal adhesions (FA) are large macromolecular assemblies which help transmit mechanical forces and regulatory signals between the extracellular matrix and an interacting cell. Two key proteins talin and vinculin connecting integrin to actomyosin networks in the cell. Both proteins bind to F-actin and each other, providing a foundation for network formation within FAs. However, the underlying mechanisms regulating their engagement remain unclear. Here, we report on the results of in vitro reconstitution of talin-vinculin-actin assemblies using synthetic membrane systems. We find that neither talin nor vinculin alone recruit actin filaments to the membrane. In contrast, phosphoinositide-rich membranes recruit and activate talin, and the membrane-bound talin then activates vinculin. Together, the two proteins then link actin to the membrane. Encapsulation of these components within vesicles reorganized actin into higher-order networks. Notably, these observations were made in the absence of applied force, whereby we infer that the initial assembly stage of FAs is force independent. Our findings demonstrate that the local membrane composition plays a key role in controlling the stepwise recruitment, activation, and engagement of proteins within FAs. |
format | Online Article Text |
id | pubmed-7384861 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-73848612020-07-29 Phosphoinositides regulate force-independent interactions between talin, vinculin, and actin Kelley, Charlotte F Litschel, Thomas Schumacher, Stephanie Dedden, Dirk Schwille, Petra Mizuno, Naoko eLife Cell Biology Focal adhesions (FA) are large macromolecular assemblies which help transmit mechanical forces and regulatory signals between the extracellular matrix and an interacting cell. Two key proteins talin and vinculin connecting integrin to actomyosin networks in the cell. Both proteins bind to F-actin and each other, providing a foundation for network formation within FAs. However, the underlying mechanisms regulating their engagement remain unclear. Here, we report on the results of in vitro reconstitution of talin-vinculin-actin assemblies using synthetic membrane systems. We find that neither talin nor vinculin alone recruit actin filaments to the membrane. In contrast, phosphoinositide-rich membranes recruit and activate talin, and the membrane-bound talin then activates vinculin. Together, the two proteins then link actin to the membrane. Encapsulation of these components within vesicles reorganized actin into higher-order networks. Notably, these observations were made in the absence of applied force, whereby we infer that the initial assembly stage of FAs is force independent. Our findings demonstrate that the local membrane composition plays a key role in controlling the stepwise recruitment, activation, and engagement of proteins within FAs. eLife Sciences Publications, Ltd 2020-07-13 /pmc/articles/PMC7384861/ /pubmed/32657269 http://dx.doi.org/10.7554/eLife.56110 Text en http://creativecommons.org/publicdomain/zero/1.0/ http://creativecommons.org/publicdomain/zero/1.0/This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication (http://creativecommons.org/publicdomain/zero/1.0/) . |
spellingShingle | Cell Biology Kelley, Charlotte F Litschel, Thomas Schumacher, Stephanie Dedden, Dirk Schwille, Petra Mizuno, Naoko Phosphoinositides regulate force-independent interactions between talin, vinculin, and actin |
title | Phosphoinositides regulate force-independent interactions between talin, vinculin, and actin |
title_full | Phosphoinositides regulate force-independent interactions between talin, vinculin, and actin |
title_fullStr | Phosphoinositides regulate force-independent interactions between talin, vinculin, and actin |
title_full_unstemmed | Phosphoinositides regulate force-independent interactions between talin, vinculin, and actin |
title_short | Phosphoinositides regulate force-independent interactions between talin, vinculin, and actin |
title_sort | phosphoinositides regulate force-independent interactions between talin, vinculin, and actin |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7384861/ https://www.ncbi.nlm.nih.gov/pubmed/32657269 http://dx.doi.org/10.7554/eLife.56110 |
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