In Vivo Proximity Labeling for the Detection of Protein-Protein and Protein-RNA Interactions

被引:19
|
作者
Beck, David B. [1 ,2 ]
Narendra, Varun [1 ,2 ]
Drury, William J., III [1 ,2 ]
Casey, Ryan [1 ,2 ]
Jansen, Pascal W. T. C. [3 ]
Yuan, Zuo-Fei [4 ]
Garcia, Benjamin A. [4 ]
Vermeulen, Michiel [3 ]
Bonasio, Roberto [5 ]
机构
[1] NYU, Sch Med, Howard Hughes Med Inst, New York, NY 10016 USA
[2] NYU, Sch Med, Dept Biochem, New York, NY 10016 USA
[3] Univ Med Ctr Utrecht, Dept Mol Canc Res, NL-3584 CG Utrecht, Netherlands
[4] Univ Penn, Perelman Sch Med, Epigenet Program, Dept Biochem & Biophys, Philadelphia, PA 19103 USA
[5] Univ Penn, Perelman Sch Med, Epigenet Program, Dept Cell & Dev Biol, Philadelphia, PA 19103 USA
基金
美国国家卫生研究院;
关键词
Proximity labeling; protein-protein interactions; protein-RNA interactions; biotinylation; covalent tag; RNA-seq; TANDEM MASS-SPECTROMETRY; PEPTIDE IDENTIFICATION; BINDING PROTEINS; NONCODING RNAS; NUCLEAR-MATRIX; CHROMATIN; COMPLEXES; CELLS; IMMUNOPRECIPITATION; RESOLUTION;
D O I
10.1021/pr500196b
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Accurate and sensitive detection of protein-protein and protein-RNA interactions is key to understanding their biological functions. Traditional methods to identify these interactions require cell lysis and biochemical manipulations that exclude cellular compartments that cannot be solubilized under mild conditions. Here, we introduce an in vivo proximity labeling (IPL) technology that employs an affinity tag combined with a photoactivatable probe to label polypeptides and RNAs in the vicinity of a protein of interest in vivo. Using quantitative mass spectrometry and deep sequencing, we show that IPL correctly identifies known protein-protein and protein-RNA interactions in the nucleus of mammalian cells. Thus, IPL provides additional temporal and spatial information for the characterization of biological interactions in vivo.
引用
收藏
页码:6135 / 6143
页数:9
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