Mass spectrometric methods to analyze the structural organization of macromolecular complexes

被引:54
作者
Rajabi, Khadijeh [1 ]
Ashcroft, Alison E. [1 ]
Radford, Sheena E. [1 ]
机构
[1] Univ Leeds, Sch Mol & Cellular Biol, Astbury Ctr Struct Mol Biol, Leeds LS2 9JT, W Yorkshire, England
基金
英国生物技术与生命科学研究理事会;
关键词
Native mass spectrometry (MS); Electrospray ionization (ESI); High mass-to-charge calibration; Fast photochemical oxidation of proteins (FPOP); Hydrogen/deuterium exchange (HDX); Cross-linking (XL); FAST PHOTOCHEMICAL OXIDATION; ION MOBILITY SPECTROMETRY; PHASE H/D EXCHANGE; CHEMICAL CROSS-LINKING; GAS-PHASE; HYDROGEN/DEUTERIUM EXCHANGE; PROTEIN IONS; ELECTROSPRAY-IONIZATION; HYDROGEN-EXCHANGE; CONFORMATIONAL-CHANGES;
D O I
10.1016/j.ymeth.2015.03.004
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
With the development of soft ionization techniques such as electrospray ionization (ESI), mass spectrometry (MS) has found widespread application in structural biology. The ability to transfer large biomolecular complexes intact into the gas-phase, combined with the low sample consumption and high sensitivity of MS, has made ESI-MS a method of choice for the characterization of macromolecules. This paper describes the application of MS to study large non-covalent complexes. We categorize the available techniques in two groups. First, solution-based techniques in which the biomolecules are labeled in solution and subsequently characterized by MS. Three MS-based techniques are discussed, namely hydroxyl radical footprinting, cross-linking and hydrogen/deuterium exchange (HDX) MS. In the second group, MS-based techniques to probe intact biomolecules in the gas-phase, e.g. side-chain microsolvation, HDX and ion mobility spectrometry are discussed. Together, the approaches place MS as a powerful methodology for an ever growing plethora of structural applications. (C) 2015 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license.
引用
收藏
页码:13 / 21
页数:9
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