Protein-Protein Interaction Detection Via Mass Spectrometry-Based Proteomics

被引:10
|
作者
Turriziani, Benedetta [1 ]
von Kriegsheim, Alexander [1 ]
Pennington, Stephen R. [2 ]
机构
[1] Univ Coll Dublin, Conway Inst, Syst Biol Ireland, Dublin 4, Ireland
[2] Univ Coll Dublin, Inst Biomol & Biomed Res, UCD Conway, Sch Med & Med Sci, Dublin 4, Ireland
关键词
Protein complex; Co-purification; Cross-linking; Co-elution; Interaction proteomics; CROSS-LINKING; QUANTITATIVE PROTEOMICS; AFFINITY PURIFICATION; CELL BIOLOGY; COMPLEXES; IDENTIFICATION; STRATEGY; SYSTEM; MS/MS;
D O I
10.1007/978-3-319-41448-5_18
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
Analysis of protein-protein interactions is one of the mainstays of mass spectrometry-based proteomics and recent developments, which have simplified the methodology, have permitted non-specialised laboratories to adopt the approach. We introduce and review three complimentary methods which allow for the targeted, global and site-specific analysis of protein complexes. Co-precipitation of endogenous or ectopically expressed proteins and their complexes followed by proteomic analysis allows for the discovery and accurate quantification of specific protein interactions. Whereas complimentary methods, such as co-purification of entire complexes based on physico-chemical attributes, can give a snapshot of the composition and dynamics of protein complexes on a global scale. Cross-linking on the other hand can pinpoint the amino acids involved in protein-protein interactions to such a resolution that the likely complex can be reconstructed computationally.
引用
收藏
页码:383 / 396
页数:14
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