Photocrosslinking approaches to interactome mapping

被引:110
作者
Pham, Nam D. [1 ]
Parker, Randy B. [1 ]
Kohler, Jennifer J. [1 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Biochem, Dallas, TX 75390 USA
基金
美国国家卫生研究院;
关键词
PROTEIN-PROTEIN INTERACTIONS; RNA-POLYMERASE-II; DIRECTED TOSYL CHEMISTRY; IN-VIVO; CELL-SURFACE; LIVING CELLS; SIALIC-ACID; TRANSCRIPTIONAL REGULATION; QUANTITATIVE PROTEOMICS; MOLECULAR CHAPERONES;
D O I
10.1016/j.cbpa.2012.10.034
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
Photocrosslinking approaches can be used to map interactome networks within the context of living cells. Photocrosslinking methods rely on use of metabolic engineering or genetic code expansion to incorporate photocrosslinking analogs of amino acids or sugars into cellular biomolecules. Immunological and mass spectrometry techniques are used to analyze crosslinked complexes, thereby defining specific interactomes. Because photocrosslinking can be conducted in native, cellular settings, it can be used to. define context-dependent interactions. Photogrosslinking methods are also ideally suited for determining interactome dynamics, mapping interaction interfaces, and identifying transient interactions in which intrinsically disordered proteins and glycoproteins engage. Here we discuss the application of cell-based photocrosslinking to the study of specific problems in immune cell signaling, transcription, membrane protein dynamics, nucleocytoplasmic transport, and chaperone-assisted protein folding.
引用
收藏
页码:90 / 101
页数:12
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