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Intracellular wetting mediates contacts between liquid compartments and membrane-bound organelles

Protein-rich droplets, such as stress granules, P-bodies, and the nucleolus, perform diverse and specialized cellular functions. Recent evidence has shown the droplets, which are also known as biomolecular condensates or membrane-less compartments, form by phase separation. Many droplets also contac...

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Detalles Bibliográficos
Autores principales: Kusumaatmaja, Halim, May, Alexander I., Knorr, Roland L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8404468/
https://www.ncbi.nlm.nih.gov/pubmed/34427635
http://dx.doi.org/10.1083/jcb.202103175
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author Kusumaatmaja, Halim
May, Alexander I.
Knorr, Roland L.
author_facet Kusumaatmaja, Halim
May, Alexander I.
Knorr, Roland L.
author_sort Kusumaatmaja, Halim
collection PubMed
description Protein-rich droplets, such as stress granules, P-bodies, and the nucleolus, perform diverse and specialized cellular functions. Recent evidence has shown the droplets, which are also known as biomolecular condensates or membrane-less compartments, form by phase separation. Many droplets also contact membrane-bound organelles, thereby functioning in development, intracellular degradation, and organization. These underappreciated interactions have major implications for our fundamental understanding of cells. Starting with a brief introduction to wetting phenomena, we summarize recent progress in the emerging field of droplet–membrane contact. We describe the physical mechanism of droplet–membrane interactions, discuss how these interactions remodel droplets and membranes, and introduce "membrane scaffolding" by liquids as a novel reshaping mechanism, thereby demonstrating that droplet–membrane interactions are elastic wetting phenomena. “Membrane-less” and “membrane-bound” condensates likely represent distinct wetting states that together link phase separation with mechanosensitivity and explain key structures observed during embryogenesis, during autophagy, and at synapses. We therefore contend that droplet wetting on membranes provides a robust and intricate means of intracellular organization.
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spelling pubmed-84044682022-04-04 Intracellular wetting mediates contacts between liquid compartments and membrane-bound organelles Kusumaatmaja, Halim May, Alexander I. Knorr, Roland L. J Cell Biol Perspective Protein-rich droplets, such as stress granules, P-bodies, and the nucleolus, perform diverse and specialized cellular functions. Recent evidence has shown the droplets, which are also known as biomolecular condensates or membrane-less compartments, form by phase separation. Many droplets also contact membrane-bound organelles, thereby functioning in development, intracellular degradation, and organization. These underappreciated interactions have major implications for our fundamental understanding of cells. Starting with a brief introduction to wetting phenomena, we summarize recent progress in the emerging field of droplet–membrane contact. We describe the physical mechanism of droplet–membrane interactions, discuss how these interactions remodel droplets and membranes, and introduce "membrane scaffolding" by liquids as a novel reshaping mechanism, thereby demonstrating that droplet–membrane interactions are elastic wetting phenomena. “Membrane-less” and “membrane-bound” condensates likely represent distinct wetting states that together link phase separation with mechanosensitivity and explain key structures observed during embryogenesis, during autophagy, and at synapses. We therefore contend that droplet wetting on membranes provides a robust and intricate means of intracellular organization. Rockefeller University Press 2021-08-24 /pmc/articles/PMC8404468/ /pubmed/34427635 http://dx.doi.org/10.1083/jcb.202103175 Text en © 2021 Kusumaatmaja et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Perspective
Kusumaatmaja, Halim
May, Alexander I.
Knorr, Roland L.
Intracellular wetting mediates contacts between liquid compartments and membrane-bound organelles
title Intracellular wetting mediates contacts between liquid compartments and membrane-bound organelles
title_full Intracellular wetting mediates contacts between liquid compartments and membrane-bound organelles
title_fullStr Intracellular wetting mediates contacts between liquid compartments and membrane-bound organelles
title_full_unstemmed Intracellular wetting mediates contacts between liquid compartments and membrane-bound organelles
title_short Intracellular wetting mediates contacts between liquid compartments and membrane-bound organelles
title_sort intracellular wetting mediates contacts between liquid compartments and membrane-bound organelles
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8404468/
https://www.ncbi.nlm.nih.gov/pubmed/34427635
http://dx.doi.org/10.1083/jcb.202103175
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