共 28 条
Chemical Cross-Linking and Mass Spectrometry As a Low-Resolution Protein Structure Determination Technique
被引:89
作者:

Singh, Pragya
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机构:
Univ Washington, Dept Med Chem, Seattle, WA 98195 USA Univ Washington, Dept Med Chem, Seattle, WA 98195 USA

Panchaud, Alexandre
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机构:
Univ Washington, Dept Med Chem, Seattle, WA 98195 USA Univ Washington, Dept Med Chem, Seattle, WA 98195 USA

Goodlett, David R.
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h-index: 0
机构:
Univ Washington, Dept Med Chem, Seattle, WA 98195 USA Univ Washington, Dept Med Chem, Seattle, WA 98195 USA
机构:
[1] Univ Washington, Dept Med Chem, Seattle, WA 98195 USA
关键词:
LINKED PEPTIDES;
LIVING CELLS;
IDENTIFICATION;
REAGENTS;
COMPLEXES;
TOOL;
DISSOCIATION;
QUATERNARY;
STRATEGY;
D O I:
10.1021/ac1000724
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
Protein complexes are the foundation of a majority of cellular processes. Although a large number of protein complexes have been identified through biochemical experiments, the precise molecular details and three-dimensional structures are available for only a small fraction. Chemical cross-linking coupled with mass spectrometry (CXMS) has gained popularity in recent years for characterization of inter- and intraprotein interactions in protein complexes. This perspective provides a comprehensive and critical overview of CMS strategies employed for structural elucidation of protein complexes. We evaluate the challenges associated with CXMS techniques with special emphasis on data analysis. As sensitivity, mass resolution, mass accuracy and ease of use of mass spectrometers have improved, the complexity of processing and interpreting CXMS data has become the central problem to be addressed. We review here a number of computer programs available to address these problems.
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页码:2636 / 2642
页数:7
相关论文
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