| Literature DB >> 28358392 |
Kevin Titeca1,2, Emmy Van Quickelberghe1,2, Noortje Samyn1,2, Delphine De Sutter1,2, Annick Verhee1,2, Kris Gevaert1,2, Jan Tavernier1,2, Sven Eyckerman1,2.
Abstract
The analysis of protein interaction networks is one of the key challenges in the study of biology. It connects genotypes to phenotypes, and disruption of such networks is associated with many pathologies. Virtually all the approaches to the study of protein complexes require cell lysis, a dramatic step that obliterates cellular integrity and profoundly affects protein interactions. This protocol starts with Virotrap, a novel approach that avoids the need for cell homogenization by fusing the protein of interest to the HIV-1 Gag protein, trapping protein complexes in virus-like particles. By using the straightforward filtering index (SFINX), which is a powerful and intuitive online tool (http://sfinx.ugent.be) that enables contaminant removal from candidate lists resulting from mass-spectrometry-based analysis, we provide a complete workflow for researchers interested in mammalian protein complexes. Given direct access to mass spectrometers, researchers can process up to 24 samples in 7 d.Entities:
Mesh:
Substances:
Year: 2017 PMID: 28358392 DOI: 10.1038/nprot.2017.014
Source DB: PubMed Journal: Nat Protoc ISSN: 1750-2799 Impact factor: 13.491