Literature DB >> 29991506

A Versatile Lentiviral Delivery Toolkit for Proximity-dependent Biotinylation in Diverse Cell Types.

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.
© 2018 Samavarchi-Tehrani et al.

Entities:  

Keywords:  Affinity proteomics; Affinity tagging; Cell biology; Cellular organelles; Molecular biology; Protein-Protein Interactions; Spectral counting

Mesh:

Substances:

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


  74 in total

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Review 8.  Protein Neighbors and Proximity Proteomics.

Authors:  Johanna S Rees; Xue-Wen Li; Sarah Perrett; Kathryn S Lilley; Antony P Jackson
Journal:  Mol Cell Proteomics       Date:  2015-09-08       Impact factor: 5.911

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Review 2.  Comprehensive Interactome Mapping of Nuclear Receptors Using Proximity Biotinylation.

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Review 5.  Recent advances in proximity-based labeling methods for interactome mapping.

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7.  Defining the interactomes of proteins involved in cytoskeletal dynamics using high-throughput proximity-dependent biotinylation in cellulo.

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