Proximity labeling to detect RNA-protein interactions in live cells

被引:12
|
作者
Lu, Mingxing [1 ]
Wei, Wencheng [2 ]
机构
[1] City Univ Hong Kong, Coll Vet Med & Life Sci, Dept Biomed Sci, Kowloon Tong, 83 Tat Chee Ave, Hong Kong 999077, Peoples R China
[2] Southern Univ Sci & Technol, Dept Biol, Shenzhen, Peoples R China
来源
FEBS OPEN BIO | 2019年 / 9卷 / 11期
关键词
APEX2; birA*; nascent peptide; proximity labeling; RNA binding protein; RNA-protein interactions; RIBONUCLEOPROTEIN COMPLEXES; BIOTIN LIGASE; IDENTIFICATION; INSIGHTS; REVEALS; LOCALIZATION; NETWORKS; CLIP;
D O I
10.1002/2211-5463.12706
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
RNA biology is orchestrated by the dynamic interactions of RNAs and RNA-binding proteins (RBPs). In the present study, we describe a new method of proximity-dependent protein labeling to detect RNA-protein interactions [RNA-bound protein proximity labeling (RBPL)]. We selected the well-studied RNA-binding protein PUF to examine the current proximity labeling enzymes birA* and APEX2. A new version of birA*, BASU, was used to validate that the PUF protein binds its RNA motif. We further optimized the RBPL labeling system using an inducible expression system. The RBPL (lambda N-BASU) labeling experiments exhibited high signal-to-noise ratios. We subsequently determined that RBPL (lambda N-BASU) is more suitable than RBPL (lambda N-APEX2) for the detection of RNA-protein interactions in live cells. Interestingly, our results also reveal that proximity labeling is probably capable of biotinylating proximate nascent peptide.
引用
收藏
页码:1860 / 1868
页数:9
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