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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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.
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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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