| Literature DB >> 30394395 |
Rongbing Huang1, Mengting Han1, Liying Meng2, Xing Chen3.
Abstract
A comprehensive identification of RNA-binding proteins (RBPs) is key to understanding the posttranscriptional regulatory network in cells. A widely used strategy for RBP capture exploits the polyadenylation [poly(A)] of target RNAs, which mostly occurs on eukaryotic mature mRNAs, leaving most binding proteins of non-poly(A) RNAs unidentified. Here we describe the detailed procedures of a recently reported method termed click chemistry-assisted RNA-interactome capture (CARIC), which enables the transcriptome-wide capture of both poly(A) and non-poly(A) RBPs by combining the metabolic labeling of RNAs, in vivo UV cross-linking, and bioorthogonal tagging.Entities:
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Year: 2018 PMID: 30394395 PMCID: PMC6235571 DOI: 10.3791/58580
Source DB: PubMed Journal: J Vis Exp ISSN: 1940-087X Impact factor: 1.355