Mass spectrometry: come of age for structural and dynamical biology

被引:224
作者
Benesch, Justin L. P. [1 ]
Ruotolo, Brandon T. [2 ]
机构
[1] Univ Oxford, Dept Chem, Phys & Theoret Chem Lab, Oxford OX1 3QZ, England
[2] Univ Michigan, Dept Chem, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院;
关键词
SURFACE-INDUCED DISSOCIATION; PROTEIN COMPLEXES; MACROMOLECULAR ASSEMBLIES; QUATERNARY ORGANIZATION; GAS-PHASE; ALZHEIMERS-DISEASE; CHAPERONE FUNCTION; REVEALS; TIME; STOICHIOMETRY;
D O I
10.1016/j.sbi.2011.08.002
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
Over the past two decades, mass spectrometry (MS) has emerged as a bone fide approach for structural biology. MS can inform on all levels of protein organization, and enables quantitative assessments of their intrinsic dynamics. The key advantages of MS are that it is a sensitive, high-resolution separation technique with wide applicability, and thereby allows the interrogation of transient protein assemblies in the context of complex mixtures. Here we describe how molecular-level information is derived from MS experiments, and how it can be combined with spatial and dynamical restraints obtained from other structural biology approaches to allow hybrid studies of protein architecture and movements.
引用
收藏
页码:641 / 649
页数:9
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