Cross-linking mass spectrometry for mapping protein complex topologies in situ

被引:29
作者
Lee, Kitaik [1 ]
O'Reilly, Francis J. [1 ]
机构
[1] NCI, Ctr Struct Biol, Ctr Canc Res, Frederick, MD 21702 USA
基金
美国国家卫生研究院;
关键词
LINKED PEPTIDES; SELECTIVE ENRICHMENT; INTERACTION NETWORK; IDENTIFICATION; INTERACTOME; PRODUCTS; CELLS; ARCHITECTURE; DYNAMICS;
D O I
10.1042/EBC20220168
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
Cross-linking mass spectrometry has become an established technology to provide struc-tural information on the topology and dynamics of protein complexes. Readily accessible workflows can provide detailed data on simplified systems, such as purified complexes. However, using this technology to study the structure of protein complexes in situ, such as in organelles, cells, and even tissues, is still a technological frontier. The complexity of these systems remains a considerable challenge, but there have been dramatic improve-ments in sample handling, data acquisition, and data processing. Here, we summarise these developments and describe the paths towards comprehensive and comparative structural interactomes by cross-linking mass spectrometry.
引用
收藏
页码:215 / 228
页数:14
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