Horizontal Cell Biology: Monitoring Global Changes of Protein Interaction States with the Proteome-Wide Cellular Thermal Shift Assay (CETSA)

被引:90
作者
Dai, Lingyun [1 ]
Prabhu, Nayana [1 ]
Yu, Liang Ying [1 ,2 ]
Bacanu, Smaranda [2 ]
Ramos, Anderson Daniel [2 ]
Nordlund, Par [1 ,2 ,3 ]
机构
[1] Nanyang Technol Univ, Sch Biol Sci, Singapore 138673, Singapore
[2] Karolinska Inst, Dept Pathol & Oncol, S-17177 Stockholm, Sweden
[3] ASTAR, Inst Mol & Cellular Biol, Singapore 138673, Singapore
来源
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 88 | 2019年 / 88卷
基金
英国医学研究理事会; 新加坡国家研究基金会;
关键词
cellular thermal shift assay; quantitative proteomics; target engagement; mechanistic biomarkers; drug development; protein interaction state; DRUG TARGET ENGAGEMENT; PHENYLALANINE-HYDROXYLASE; MASS-SPECTROMETRY; OFF-TARGET; IDENTIFICATION; STABILITY; FERROCHELATASE; QUANTIFICATION; PANOBINOSTAT; ACTIVATION;
D O I
10.1146/annurev-biochem-062917-012837
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
The cellular thermal shift assay (CETSA) is a biophysical technique allowing direct studies of ligand binding to proteins in cells and tissues. The proteome-wide implementation of CETSA with mass spectrometry detection (MS-CETSA) has now been successfully applied to discover targets for orphan clinical drugs and hits from phenotypic screens, to identify offtargets, and to explain poly-pharmacology and drug toxicity. Highly sensitive multidimensional MS-CETSA implementations can now also access binding of physiological ligands to proteins, such as metabolites, nucleic acids, and other proteins. MS-CETSA can thereby provide comprehensive information on modulations of protein interaction states in cellular processes, including downstream effects of drugs and transitions between different physiological cell states. Such horizontal information on ligand modulation in cells is largely orthogonal to vertical information on the levels of different proteins and therefore opens novel opportunities to understand operational aspects of cellular proteomes.
引用
收藏
页码:383 / 408
页数:26
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