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Aging can transform single-component protein condensates into multiphase architectures

Phase-separated biomolecular condensates that contain multiple coexisting phases are widespread in vitro and in cells. Multiphase condensates emerge readily within multicomponent mixtures of biomolecules (e.g., proteins and nucleic acids) when the different components present sufficient physicochemi...

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Autores principales: Garaizar, Adiran, Espinosa, Jorge R., Joseph, Jerelle A., Krainer, Georg, Shen, Yi, Knowles, Tuomas P.J., Collepardo-Guevara, Rosana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9245653/
https://www.ncbi.nlm.nih.gov/pubmed/35727989
http://dx.doi.org/10.1073/pnas.2119800119
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author Garaizar, Adiran
Espinosa, Jorge R.
Joseph, Jerelle A.
Krainer, Georg
Shen, Yi
Knowles, Tuomas P.J.
Collepardo-Guevara, Rosana
author_facet Garaizar, Adiran
Espinosa, Jorge R.
Joseph, Jerelle A.
Krainer, Georg
Shen, Yi
Knowles, Tuomas P.J.
Collepardo-Guevara, Rosana
author_sort Garaizar, Adiran
collection PubMed
description Phase-separated biomolecular condensates that contain multiple coexisting phases are widespread in vitro and in cells. Multiphase condensates emerge readily within multicomponent mixtures of biomolecules (e.g., proteins and nucleic acids) when the different components present sufficient physicochemical diversity (e.g., in intermolecular forces, structure, and chemical composition) to sustain separate coexisting phases. Because such diversity is highly coupled to the solution conditions (e.g., temperature, pH, salt, composition), it can manifest itself immediately from the nucleation and growth stages of condensate formation, develop spontaneously due to external stimuli or emerge progressively as the condensates age. Here, we investigate thermodynamic factors that can explain the progressive intrinsic transformation of single-component condensates into multiphase architectures during the nonequilibrium process of aging. We develop a multiscale model that integrates atomistic simulations of proteins, sequence-dependent coarse-grained simulations of condensates, and a minimal model of dynamically aging condensates with nonconservative intermolecular forces. Our nonequilibrium simulations of condensate aging predict that single-component condensates that are initially homogeneous and liquid like can transform into gel-core/liquid-shell or liquid-core/gel-shell multiphase condensates as they age due to gradual and irreversible enhancement of interprotein interactions. The type of multiphase architecture is determined by the aging mechanism, the molecular organization of the gel and liquid phases, and the chemical makeup of the protein. Notably, we predict that interprotein disorder to order transitions within the prion-like domains of intracellular proteins can lead to the required nonconservative enhancement of intermolecular interactions. Our study, therefore, predicts a potential mechanism by which the nonequilibrium process of aging results in single-component multiphase condensates.
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spelling pubmed-92456532022-12-21 Aging can transform single-component protein condensates into multiphase architectures Garaizar, Adiran Espinosa, Jorge R. Joseph, Jerelle A. Krainer, Georg Shen, Yi Knowles, Tuomas P.J. Collepardo-Guevara, Rosana Proc Natl Acad Sci U S A Biological Sciences Phase-separated biomolecular condensates that contain multiple coexisting phases are widespread in vitro and in cells. Multiphase condensates emerge readily within multicomponent mixtures of biomolecules (e.g., proteins and nucleic acids) when the different components present sufficient physicochemical diversity (e.g., in intermolecular forces, structure, and chemical composition) to sustain separate coexisting phases. Because such diversity is highly coupled to the solution conditions (e.g., temperature, pH, salt, composition), it can manifest itself immediately from the nucleation and growth stages of condensate formation, develop spontaneously due to external stimuli or emerge progressively as the condensates age. Here, we investigate thermodynamic factors that can explain the progressive intrinsic transformation of single-component condensates into multiphase architectures during the nonequilibrium process of aging. We develop a multiscale model that integrates atomistic simulations of proteins, sequence-dependent coarse-grained simulations of condensates, and a minimal model of dynamically aging condensates with nonconservative intermolecular forces. Our nonequilibrium simulations of condensate aging predict that single-component condensates that are initially homogeneous and liquid like can transform into gel-core/liquid-shell or liquid-core/gel-shell multiphase condensates as they age due to gradual and irreversible enhancement of interprotein interactions. The type of multiphase architecture is determined by the aging mechanism, the molecular organization of the gel and liquid phases, and the chemical makeup of the protein. Notably, we predict that interprotein disorder to order transitions within the prion-like domains of intracellular proteins can lead to the required nonconservative enhancement of intermolecular interactions. Our study, therefore, predicts a potential mechanism by which the nonequilibrium process of aging results in single-component multiphase condensates. National Academy of Sciences 2022-06-21 2022-06-28 /pmc/articles/PMC9245653/ /pubmed/35727989 http://dx.doi.org/10.1073/pnas.2119800119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Garaizar, Adiran
Espinosa, Jorge R.
Joseph, Jerelle A.
Krainer, Georg
Shen, Yi
Knowles, Tuomas P.J.
Collepardo-Guevara, Rosana
Aging can transform single-component protein condensates into multiphase architectures
title Aging can transform single-component protein condensates into multiphase architectures
title_full Aging can transform single-component protein condensates into multiphase architectures
title_fullStr Aging can transform single-component protein condensates into multiphase architectures
title_full_unstemmed Aging can transform single-component protein condensates into multiphase architectures
title_short Aging can transform single-component protein condensates into multiphase architectures
title_sort aging can transform single-component protein condensates into multiphase architectures
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9245653/
https://www.ncbi.nlm.nih.gov/pubmed/35727989
http://dx.doi.org/10.1073/pnas.2119800119
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