The beginning of a beautiful friendship: Cross-linking/mass spectrometry and modelling of proteins and multi-protein complexes

被引:325
作者
Rappsilber, Juri [1 ]
机构
[1] Univ Edinburgh, Wellcome Trust Ctr Cell Biol, Edinburgh EH9 3JR, Midlothian, Scotland
基金
英国惠康基金;
关键词
Cross-linking; Mass spectrometry; Modelling; Integrated structural biology; Multi-protein complexes; COLLISION-INDUCED DISSOCIATION; MASS-SPECTRAL DATA; RNA-POLYMERASE-II; LINKED PEPTIDES; GAS-PHASE; MACROMOLECULAR ASSEMBLIES; SELECTIVE ENRICHMENT; ALLOW IDENTIFICATION; STRUCTURAL-ANALYSIS; ESCHERICHIA-COLI;
D O I
10.1016/j.jsb.2010.10.014
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
After more than a decade of method development, cross-linking in combination with mass spectrometry and bioinformatics is finally coming of age. This technology now provides improved opportunities for modelling by mapping structural details of functional complexes in solution. The structure of proteins or protein complexes is ascertained by identifying amino acid pairs that are positioned in close proximity to each other. The validity of this technique has recently been benchmarked for large multi-protein complexes, by comparing cross-link data with that from a crystal structure of RNA polymerase II. Here, the specific nature of this cross-linking data will be discussed to assess the technical challenges and opportunities for model building. We believe that once remaining technological challenges of cross-linking/mass spectrometry have been addressed and cross-linking/mass spectrometry data has been incorporated into modelling algorithms it will quickly become an indispensable companion of protein and protein complex modelling and a corner-stone of integrated structural biology. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:530 / 540
页数:11
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