Developments in rapid hydrogen-deuterium exchange methods

被引:8
|
作者
Chow, Vimanda [1 ]
Wolf, Esther [1 ]
Lento, Cristina [1 ]
Wilson, Derek J. [1 ]
机构
[1] York Univ, Dept Chem, Toronto, ON M3J 1P3, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
PHASE H/D EXCHANGE; INTRINSICALLY DISORDERED PROTEINS; ELECTRON-TRANSFER DISSOCIATION; MASS-SPECTROMETRIC ANALYSIS; HIGHER-ORDER STRUCTURE; HYDROGEN/DEUTERIUM-EXCHANGE; GAS-PHASE; CONFORMATIONAL DYNAMICS; RESOLUTION; REGIONS;
D O I
10.1042/EBC20220174
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
Biological macromolecules, such as proteins, nucleic acids, and carbohydrates, con-tain heteroatom-bonded hydrogens that undergo exchange with solvent hydrogens on timescales ranging from microseconds to hours. In hydrogen-deuterium exchange mass spectrometry (HDX-MS), this exchange process is used to extract information about biomolecular structure and dynamics. This minireview focuses on millisecond timescale HDX-MS measurements, which, while less common than 'conventional' timescale (seconds to hours) HDX-MS, provide a unique window into weakly structured species, weak (or fast cycling) binding interactions, and subtle shifts in conformational dynamics. This includes in-trinsically disordered proteins and regions (IDPs/IDRs) that are associated with cancer and amyloidotic neurodegenerative disease. For nucleic acids and carbohydrates, structures such as isomers, stems, and loops, can be elucidated and overall structural rigidity can be assessed. We will provide a brief overview of technical developments in rapid HDX followed by highlights of various applications, emphasising the importance of broadening the HDX timescale to improve throughput and to capture a wider range of function-relevant dynamic and structural shifts.
引用
收藏
页码:165 / 174
页数:10
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