Two decades of studying non-covalent biomolecular assemblies by means of electrospray ionization mass spectrometry

被引:118
作者
Hilton, Gillian R.
Benesch, Justin L. P. [1 ]
机构
[1] Univ Oxford, Dept Chem Phys, Oxford OX3 1QZ, England
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
mass spectrometry; ion mobility; protein assembly; non-covalent complex; hybrid structural biology; PROTEIN COMPLEXES REVEALS; ION MOBILITY SPECTROMETRY; ALPHA-B-CRYSTALLIN; GAS-PHASE; QUATERNARY ORGANIZATION; CONFORMATIONAL-CHANGES; SUBUNIT ARCHITECTURE; RANGE QUADRUPOLE; LIGAND-BINDING; CROSS-SECTIONS;
D O I
10.1098/rsif.2011.0823
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mass spectrometry (MS) is a recognized approach for characterizing proteins and the complexes they assemble into. This application of a long-established physico-chemical tool to the frontiers of structural biology has stemmed from experiments performed in the early 1990s. While initial studies focused on the elucidation of stoichiometry by means of simple mass determination, developments in MS technology and methodology now allow researchers to address questions of shape, inter-subunit connectivity and protein dynamics. Here, we chart the remarkable rise of MS and its application to biomolecular complexes over the last two decades.
引用
收藏
页码:801 / 816
页数:16
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