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Application of shotgun proteomics for discovery-driven protein-protein interaction.

Authors :
Goto-Silva L
Maliga Z
Slabicki M
Murillo JR
Junqueira M
Source :
Methods in molecular biology (Clifton, N.J.) [Methods Mol Biol] 2014; Vol. 1156, pp. 265-78.
Publication Year :
2014

Abstract

Affinity purification of protein complexes and identification of co-purified proteins by mass spectrometry is a powerful method to discover novel protein-protein interactions. Application of this method to the study of biological systems often requires the ability to process a large number of samples. Hence, there is great need to generate proteomic workflows compatible with large-scale studies. The major goal of this protocol is to present a fast, reliable, and scalable method to characterize protein complexes by mass spectrometry to overcome the limitations of conventional geLC-MS/MS or MudPIT protocols. This method was successfully employed for the discovery and characterization of novel protein complexes in cultured yeast, mammalian cells, and mice.

Details

Language :
English
ISSN :
1940-6029
Volume :
1156
Database :
MEDLINE
Journal :
Methods in molecular biology (Clifton, N.J.)
Publication Type :
Academic Journal
Accession number :
24791995
Full Text :
https://doi.org/10.1007/978-1-4939-0685-7_18