| Literature DB >> 29991506 |
Payman Samavarchi-Tehrani1, Hala Abdouni1, Reuben Samson1,2, Anne-Claude Gingras3,2.
Abstract
Proximity-dependent biotinylation strategies have emerged as powerful tools to characterize the subcellular context of proteins in living cells. The popular BioID approach employs an abortive E. coli biotin ligase mutant (R118G; denoted as BirA*), which when fused to a bait protein enables the covalent biotinylation of endogenous proximal polypeptides. This approach has been mainly applied to the study of protein proximity in immortalized mammalian cell lines. To expand the application space of BioID, here we describe a set of lentiviral vectors that enable the inducible expression of BirA*-tagged bait fusion proteins for performing proximity-dependent biotinylation in diverse experimental systems. We benchmark this highly adaptable toolkit across immortalized and primary cell systems, demonstrating the ease, versatility and robustness of the system. We also provide guidelines to perform BioID using these reagents.Entities:
Keywords: Affinity proteomics; Affinity tagging; Cell biology; Cellular organelles; Molecular biology; Protein-Protein Interactions; Spectral counting
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Year: 2018 PMID: 29991506 PMCID: PMC6210231 DOI: 10.1074/mcp.TIR118.000902
Source DB: PubMed Journal: Mol Cell Proteomics ISSN: 1535-9476 Impact factor: 5.911