Cross-linking mass spectrometry: methods and applications in structural, molecular and systems biology

被引:211
|
作者
O'Reilly, Francis J. [1 ,2 ]
Rappsilber, Juri [1 ,2 ]
机构
[1] Tech Univ Berlin, Inst Biotechnol, Bioanalyt, Berlin, Germany
[2] Univ Edinburgh, Wellcome Ctr Cell Biol, Edinburgh, Midlothian, Scotland
基金
英国惠康基金;
关键词
PROTEIN-PROTEIN INTERACTIONS; NUCLEAR-PORE COMPLEX; EUKARYOTIC CHAPERONIN TRIC/CCT; LINKED PEPTIDES; SACCHAROMYCES-CEREVISIAE; ALLOW IDENTIFICATION; INITIATION COMPLEX; 26S PROTEASOME; SOFTWARE SUITE; LIVING CELLS;
D O I
10.1038/s41594-018-0147-0
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 decade, cross-linking mass spectrometry (CLMS) has developed into a robust and flexible tool that provides medium-resolution structural information. CLMS data provide a measure of the proximity of amino acid residues and thus offer information on the folds of proteins and the topology of their complexes. Here, we highlight notable successes of this technique as well as common pipelines. Novel CLMS applications, such as in-cell cross-linking, probing conformational changes and tertiary-structure determination, are now beginning to make contributions to molecular biology and the emerging fields of structural systems biology and interactomics.
引用
收藏
页码:1000 / 1008
页数:9
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