Mass spectrometric approaches for profiling protein folding and stability

被引:2
作者
Genereux, Joseph C. [1 ]
机构
[1] Univ Calif Riverside, Dept Chem, Riverside, CA 92521 USA
来源
PROTEIN MISFOLDING | 2020年 / 118卷
关键词
FAST PHOTOCHEMICAL OXIDATION; THERMODYNAMIC ANALYSIS; PROTEOMICS APPROACH; STRUCTURAL-ANALYSIS; GLOBAL ANALYSIS; HIGH-RESOLUTION; CROSS-LINKERS; PEPTIDE; QUANTIFICATION; BINDING;
D O I
10.1016/bs.apcsb.2019.09.006
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 stability reports on protein homeostasis, function, and binding interactions, such as to other proteins, metabolites and drugs. As such, there is a pressing need for technologies that can report on protein stability. The ideal technique could be applied in vitro or in vivo systems, proteome-wide, independently of matrix, under native conditions, with residue-level resolution, and on protein at endogenous levels. Mass spectrometry has rapidly become a preferred technology for identifying and quantifying proteins. As such, it has been increasingly incorporated into methodologies for interrogating protein stability and folding. Although no single technology can satisfy all desired applications, several emerging approaches have shown outstanding success at providing biological insight into the stability of the proteome. This chapter outlines some of these recent emerging technologies.
引用
收藏
页码:111 / 144
页数:34
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