Chemical Biology Toolbox to Visualize Protein Aggregation in Live Cells

被引:10
|
作者
Shen, Di [1 ]
Bai, Yulong [1 ,2 ]
Liu, Yu [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, CAS Key Lab Separat Sci Analyt Chem, 457 Zhongshan Rd, Dalian 116023, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
AggTag; fluorescent protein; protein aggregation; proteostasis capacity sensors; small-molecule probes; PHASE-SEPARATION; FLUOROGENIC PROBES; FLUORESCENT-PROBE; PROTEOSTASIS; OLIGOMERS; STRESS; INHIBITION; TRACKING; MUTANTS; BODIPY;
D O I
10.1002/cbic.202100443
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Protein misfolding and aggregation is a complex biochemical process and has been associated with numerous human degenerative diseases. Developing novel chemical and biological tools and approaches to visualize aggregated proteins in live cells is in high demand for mechanistic studies, diagnostics, and therapeutics. In this review, we summarize the recent developments in the chemical biology toolbox applied to protein aggregation studies in live cells. These methods exploited fluorescent protein tags, fluorescent chemical tags, and small-molecule probes to visualize the protein-aggregation process, detect proteome stresses, and quantify the protein homeostasis network capacity. Inspired by these seminal works, we have generalized design principles for the development of new detection methods and probes in the future that will illuminate this important biological process.
引用
收藏
页数:12
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