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Geometric pinning and antimixing in scaffolded lipid vesicles

Previous studies on the phase behaviour of multicomponent lipid bilayers found an intricate interplay between membrane geometry and its composition, but a fundamental understanding of curvature-induced effects remains elusive. Thanks to a combination of experiments on lipid vesicles supported by col...

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Autores principales: Rinaldin, Melissa, Fonda, Piermarco, Giomi, Luca, Kraft, Daniela J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7474073/
https://www.ncbi.nlm.nih.gov/pubmed/32887878
http://dx.doi.org/10.1038/s41467-020-17432-w
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author Rinaldin, Melissa
Fonda, Piermarco
Giomi, Luca
Kraft, Daniela J.
author_facet Rinaldin, Melissa
Fonda, Piermarco
Giomi, Luca
Kraft, Daniela J.
author_sort Rinaldin, Melissa
collection PubMed
description Previous studies on the phase behaviour of multicomponent lipid bilayers found an intricate interplay between membrane geometry and its composition, but a fundamental understanding of curvature-induced effects remains elusive. Thanks to a combination of experiments on lipid vesicles supported by colloidal scaffolds and theoretical work, we demonstrate that the local geometry and global chemical composition of the bilayer determine both the spatial arrangement and the amount of mixing of the lipids. In the mixed phase, a strong geometrical anisotropy can give rise to an antimixed state, where the lipids are mixed, but their relative concentration varies across the membrane. After phase separation, the bilayer organizes in multiple lipid domains, whose location is pinned in specific regions, depending on the substrate curvature and the bending rigidity of the lipid domains. Our results provide critical insights into the phase separation of cellular membranes and, more generally, two-dimensional fluids on curved substrates.
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spelling pubmed-74740732020-09-16 Geometric pinning and antimixing in scaffolded lipid vesicles Rinaldin, Melissa Fonda, Piermarco Giomi, Luca Kraft, Daniela J. Nat Commun Article Previous studies on the phase behaviour of multicomponent lipid bilayers found an intricate interplay between membrane geometry and its composition, but a fundamental understanding of curvature-induced effects remains elusive. Thanks to a combination of experiments on lipid vesicles supported by colloidal scaffolds and theoretical work, we demonstrate that the local geometry and global chemical composition of the bilayer determine both the spatial arrangement and the amount of mixing of the lipids. In the mixed phase, a strong geometrical anisotropy can give rise to an antimixed state, where the lipids are mixed, but their relative concentration varies across the membrane. After phase separation, the bilayer organizes in multiple lipid domains, whose location is pinned in specific regions, depending on the substrate curvature and the bending rigidity of the lipid domains. Our results provide critical insights into the phase separation of cellular membranes and, more generally, two-dimensional fluids on curved substrates. Nature Publishing Group UK 2020-09-04 /pmc/articles/PMC7474073/ /pubmed/32887878 http://dx.doi.org/10.1038/s41467-020-17432-w Text en © The Author(s) 2020 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
Rinaldin, Melissa
Fonda, Piermarco
Giomi, Luca
Kraft, Daniela J.
Geometric pinning and antimixing in scaffolded lipid vesicles
title Geometric pinning and antimixing in scaffolded lipid vesicles
title_full Geometric pinning and antimixing in scaffolded lipid vesicles
title_fullStr Geometric pinning and antimixing in scaffolded lipid vesicles
title_full_unstemmed Geometric pinning and antimixing in scaffolded lipid vesicles
title_short Geometric pinning and antimixing in scaffolded lipid vesicles
title_sort geometric pinning and antimixing in scaffolded lipid vesicles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7474073/
https://www.ncbi.nlm.nih.gov/pubmed/32887878
http://dx.doi.org/10.1038/s41467-020-17432-w
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