4.5 Review

Unravelling the microscopic characteristics of intrinsically disordered proteins upon liquid-liquid phase separation

期刊

ESSAYS IN BIOCHEMISTRY
卷 66, 期 7, 页码 891-900

出版社

PORTLAND PRESS LTD
DOI: 10.1042/EBC20220148

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资金

  1. National Natural Science Foundation of China
  2. China Postdoctoral Science Foundation
  3. CAS Centre of Excellence in Biomacromolecules
  4. [31920103011]
  5. [32171443]
  6. [2022TQ0357]

向作者/读者索取更多资源

Biomolecular condensate formation through liquid-liquid phase separation (LLPS) is a ubiquitous mechanism in the cell that organizes biomolecules spatially and temporally. This review summarizes recent biophysical studies on the intramolecular conformational changes of intrinsically disordered proteins (IDPs) and the intermolecular clustering of proteins involved in LLPS, with a focus on single-molecule fluorescence detection. The connection between these microscopic features and the macroscopic phase transitions relevant to the physiological and pathological roles of condensates is also discussed.
Biomolecular condensate formation via liquid-liquid phase separation (LLPS) has emerged as a ubiquitous mechanism underlying the spatiotemporal organization of biomolecules in the cell. These membraneless condensates form and disperse dynamically in response to environmental stimuli. Growing evidence indicates that the liquid-like condensates not only play functional physiological roles but are also implicated in a wide range of human diseases. As a major component of biomolecular condensates, intrinsically disordered proteins (IDPs) are intimately involved in the LLPS process. During the last decade, great efforts have been made on the macroscopic characterization of the physicochemical properties and biological functions of liquid condensates both in vitro and in the cellular context. However, characterization of the conformations and interactions at the molecular level within phase-separated condensates is still at an early stage. In the present review, we summarize recent biophysical studies investigating the intramolecular conformational changes of IDPs upon LLPS and the intermolecular clustering of proteins undergoing LLPS, with a particular focus on single-molecule fluorescence detection. We also discuss how these microscopic features are linked to the macroscopic phase transitions that are relevant to the physiological and pathological roles of the condensates.

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