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Wetting and complex remodeling of membranes by biomolecular condensates
Cells compartmentalize parts of their interiors into liquid-like condensates, which can be reconstituted in vitro. Although these condensates interact with membrane-bound organelles, their potential for membrane remodeling and the underlying mechanisms of such interactions are not well-understood. H...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10203268/ https://www.ncbi.nlm.nih.gov/pubmed/37217523 http://dx.doi.org/10.1038/s41467-023-37955-2 |
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author | Mangiarotti, Agustín Chen, Nannan Zhao, Ziliang Lipowsky, Reinhard Dimova, Rumiana |
author_facet | Mangiarotti, Agustín Chen, Nannan Zhao, Ziliang Lipowsky, Reinhard Dimova, Rumiana |
author_sort | Mangiarotti, Agustín |
collection | PubMed |
description | Cells compartmentalize parts of their interiors into liquid-like condensates, which can be reconstituted in vitro. Although these condensates interact with membrane-bound organelles, their potential for membrane remodeling and the underlying mechanisms of such interactions are not well-understood. Here, we demonstrate that interactions between protein condensates - including hollow ones, and membranes can lead to remarkable morphological transformations and provide a theoretical framework to describe them. Modulation of solution salinity or membrane composition drives the condensate-membrane system through two wetting transitions, from dewetting, through a broad regime of partial wetting, to complete wetting. When sufficient membrane area is available, fingering or ruffling of the condensate-membrane interface is observed, an intriguing phenomenon producing intricately curved structures. The observed morphologies are governed by the interplay of adhesion, membrane elasticity, and interfacial tension. Our results highlight the relevance of wetting in cell biology, and pave the way for the design of synthetic membrane-droplet based biomaterials and compartments with tunable properties. |
format | Online Article Text |
id | pubmed-10203268 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-102032682023-05-24 Wetting and complex remodeling of membranes by biomolecular condensates Mangiarotti, Agustín Chen, Nannan Zhao, Ziliang Lipowsky, Reinhard Dimova, Rumiana Nat Commun Article Cells compartmentalize parts of their interiors into liquid-like condensates, which can be reconstituted in vitro. Although these condensates interact with membrane-bound organelles, their potential for membrane remodeling and the underlying mechanisms of such interactions are not well-understood. Here, we demonstrate that interactions between protein condensates - including hollow ones, and membranes can lead to remarkable morphological transformations and provide a theoretical framework to describe them. Modulation of solution salinity or membrane composition drives the condensate-membrane system through two wetting transitions, from dewetting, through a broad regime of partial wetting, to complete wetting. When sufficient membrane area is available, fingering or ruffling of the condensate-membrane interface is observed, an intriguing phenomenon producing intricately curved structures. The observed morphologies are governed by the interplay of adhesion, membrane elasticity, and interfacial tension. Our results highlight the relevance of wetting in cell biology, and pave the way for the design of synthetic membrane-droplet based biomaterials and compartments with tunable properties. Nature Publishing Group UK 2023-05-22 /pmc/articles/PMC10203268/ /pubmed/37217523 http://dx.doi.org/10.1038/s41467-023-37955-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Mangiarotti, Agustín Chen, Nannan Zhao, Ziliang Lipowsky, Reinhard Dimova, Rumiana Wetting and complex remodeling of membranes by biomolecular condensates |
title | Wetting and complex remodeling of membranes by biomolecular condensates |
title_full | Wetting and complex remodeling of membranes by biomolecular condensates |
title_fullStr | Wetting and complex remodeling of membranes by biomolecular condensates |
title_full_unstemmed | Wetting and complex remodeling of membranes by biomolecular condensates |
title_short | Wetting and complex remodeling of membranes by biomolecular condensates |
title_sort | wetting and complex remodeling of membranes by biomolecular condensates |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10203268/ https://www.ncbi.nlm.nih.gov/pubmed/37217523 http://dx.doi.org/10.1038/s41467-023-37955-2 |
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