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Membrane reshaping by micrometric curvature sensitive septin filaments
Septins are cytoskeletal filaments that assemble at the inner face of the plasma membrane. They are localized at constriction sites and impact membrane remodeling. We report in vitro tools to examine how yeast septins behave on curved and deformable membranes. Septins reshape the membranes of Giant...
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/PMC6345803/ https://www.ncbi.nlm.nih.gov/pubmed/30679428 http://dx.doi.org/10.1038/s41467-019-08344-5 |
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author | Beber, Alexandre Taveneau, Cyntia Nania, Manuela Tsai, Feng-Ching Di Cicco, Aurelie Bassereau, Patricia Lévy, Daniel Cabral, João T. Isambert, Hervé Mangenot, Stéphanie Bertin, Aurélie |
author_facet | Beber, Alexandre Taveneau, Cyntia Nania, Manuela Tsai, Feng-Ching Di Cicco, Aurelie Bassereau, Patricia Lévy, Daniel Cabral, João T. Isambert, Hervé Mangenot, Stéphanie Bertin, Aurélie |
author_sort | Beber, Alexandre |
collection | PubMed |
description | Septins are cytoskeletal filaments that assemble at the inner face of the plasma membrane. They are localized at constriction sites and impact membrane remodeling. We report in vitro tools to examine how yeast septins behave on curved and deformable membranes. Septins reshape the membranes of Giant Unilamellar Vesicles with the formation of periodic spikes, while flattening smaller vesicles. We show that membrane deformations are associated to preferential arrangement of septin filaments on specific curvatures. When binding to bilayers supported on custom-designed periodic wavy patterns displaying positive and negative micrometric radii of curvatures, septin filaments remain straight and perpendicular to the curvature of the convex parts, while bending negatively to follow concave geometries. Based on these results, we propose a theoretical model that describes the deformations and micrometric curvature sensitivity observed in vitro. The model captures the reorganizations of septin filaments throughout cytokinesis in vivo, providing mechanistic insights into cell division. |
format | Online Article Text |
id | pubmed-6345803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63458032019-01-28 Membrane reshaping by micrometric curvature sensitive septin filaments Beber, Alexandre Taveneau, Cyntia Nania, Manuela Tsai, Feng-Ching Di Cicco, Aurelie Bassereau, Patricia Lévy, Daniel Cabral, João T. Isambert, Hervé Mangenot, Stéphanie Bertin, Aurélie Nat Commun Article Septins are cytoskeletal filaments that assemble at the inner face of the plasma membrane. They are localized at constriction sites and impact membrane remodeling. We report in vitro tools to examine how yeast septins behave on curved and deformable membranes. Septins reshape the membranes of Giant Unilamellar Vesicles with the formation of periodic spikes, while flattening smaller vesicles. We show that membrane deformations are associated to preferential arrangement of septin filaments on specific curvatures. When binding to bilayers supported on custom-designed periodic wavy patterns displaying positive and negative micrometric radii of curvatures, septin filaments remain straight and perpendicular to the curvature of the convex parts, while bending negatively to follow concave geometries. Based on these results, we propose a theoretical model that describes the deformations and micrometric curvature sensitivity observed in vitro. The model captures the reorganizations of septin filaments throughout cytokinesis in vivo, providing mechanistic insights into cell division. Nature Publishing Group UK 2019-01-24 /pmc/articles/PMC6345803/ /pubmed/30679428 http://dx.doi.org/10.1038/s41467-019-08344-5 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 Beber, Alexandre Taveneau, Cyntia Nania, Manuela Tsai, Feng-Ching Di Cicco, Aurelie Bassereau, Patricia Lévy, Daniel Cabral, João T. Isambert, Hervé Mangenot, Stéphanie Bertin, Aurélie Membrane reshaping by micrometric curvature sensitive septin filaments |
title | Membrane reshaping by micrometric curvature sensitive septin filaments |
title_full | Membrane reshaping by micrometric curvature sensitive septin filaments |
title_fullStr | Membrane reshaping by micrometric curvature sensitive septin filaments |
title_full_unstemmed | Membrane reshaping by micrometric curvature sensitive septin filaments |
title_short | Membrane reshaping by micrometric curvature sensitive septin filaments |
title_sort | membrane reshaping by micrometric curvature sensitive septin filaments |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6345803/ https://www.ncbi.nlm.nih.gov/pubmed/30679428 http://dx.doi.org/10.1038/s41467-019-08344-5 |
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