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Two-dimensional molecular condensation in cell signaling and mechanosensing: 2D-condensates as signaling hubs

Membraneless organelles (MLO) regulate diverse biological processes in a spatiotemporally controlled manner spanning from inside to outside of the cells. The plasma membrane (PM) at the cell surface serves as a central platform for forming multi-component signaling hubs that sense mechanical and che...

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Detalles Bibliográficos
Autores principales: Guo, Xiangfu, Zhu, Kexin, Zhu, Xinlu, Zhao, Wenting, Miao, Yansong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423693/
https://www.ncbi.nlm.nih.gov/pubmed/37475548
http://dx.doi.org/10.3724/abbs.2023132
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author Guo, Xiangfu
Zhu, Kexin
Zhu, Xinlu
Zhao, Wenting
Miao, Yansong
author_facet Guo, Xiangfu
Zhu, Kexin
Zhu, Xinlu
Zhao, Wenting
Miao, Yansong
author_sort Guo, Xiangfu
collection PubMed
description Membraneless organelles (MLO) regulate diverse biological processes in a spatiotemporally controlled manner spanning from inside to outside of the cells. The plasma membrane (PM) at the cell surface serves as a central platform for forming multi-component signaling hubs that sense mechanical and chemical cues during physiological and pathological conditions. During signal transduction, the assembly and formation of membrane-bound MLO are dynamically tunable depending on the physicochemical properties of the surrounding environment and partitioning biomolecules. Biomechanical properties of MLO-associated membrane structures can control the microenvironment for biomolecular interactions and assembly. Lipid-protein complex interactions determine the catalytic region’s assembly pattern and assembly rate and, thereby, the amplitude of activities. In this review, we will focus on how cell surface microenvironments, including membrane curvature, surface topology and tension, lipid-phase separation, and adhesion force, guide the assembly of PM-associated MLO for cell signal transductions.
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spelling pubmed-104236932023-08-15 Two-dimensional molecular condensation in cell signaling and mechanosensing: 2D-condensates as signaling hubs Guo, Xiangfu Zhu, Kexin Zhu, Xinlu Zhao, Wenting Miao, Yansong Acta Biochim Biophys Sin (Shanghai) Research Article Membraneless organelles (MLO) regulate diverse biological processes in a spatiotemporally controlled manner spanning from inside to outside of the cells. The plasma membrane (PM) at the cell surface serves as a central platform for forming multi-component signaling hubs that sense mechanical and chemical cues during physiological and pathological conditions. During signal transduction, the assembly and formation of membrane-bound MLO are dynamically tunable depending on the physicochemical properties of the surrounding environment and partitioning biomolecules. Biomechanical properties of MLO-associated membrane structures can control the microenvironment for biomolecular interactions and assembly. Lipid-protein complex interactions determine the catalytic region’s assembly pattern and assembly rate and, thereby, the amplitude of activities. In this review, we will focus on how cell surface microenvironments, including membrane curvature, surface topology and tension, lipid-phase separation, and adhesion force, guide the assembly of PM-associated MLO for cell signal transductions. Oxford University Press 2023-07-20 /pmc/articles/PMC10423693/ /pubmed/37475548 http://dx.doi.org/10.3724/abbs.2023132 Text en © The Author(s) 2021. 0 https://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Guo, Xiangfu
Zhu, Kexin
Zhu, Xinlu
Zhao, Wenting
Miao, Yansong
Two-dimensional molecular condensation in cell signaling and mechanosensing: 2D-condensates as signaling hubs
title Two-dimensional molecular condensation in cell signaling and mechanosensing: 2D-condensates as signaling hubs
title_full Two-dimensional molecular condensation in cell signaling and mechanosensing: 2D-condensates as signaling hubs
title_fullStr Two-dimensional molecular condensation in cell signaling and mechanosensing: 2D-condensates as signaling hubs
title_full_unstemmed Two-dimensional molecular condensation in cell signaling and mechanosensing: 2D-condensates as signaling hubs
title_short Two-dimensional molecular condensation in cell signaling and mechanosensing: 2D-condensates as signaling hubs
title_sort two-dimensional molecular condensation in cell signaling and mechanosensing: 2d-condensates as signaling hubs
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423693/
https://www.ncbi.nlm.nih.gov/pubmed/37475548
http://dx.doi.org/10.3724/abbs.2023132
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