High-throughput approaches to profile RNA-protein interactions

被引:31
|
作者
Nechay, Misha [1 ]
Kleiner, Ralph E. [1 ]
机构
[1] Princeton Univ, Dept Chem, Princeton, NJ 08544 USA
关键词
Ribonomics; Transcriptomics; Proteomics; CLIP; TRANSCRIPTOME-WIDE DISCOVERY; HETEROGENEOUS NUCLEAR-RNA; BINDING SITES; BOUND PROTEOME; CROSS-LINKING; IDENTIFICATION; RESOLUTION; RIBONUCLEOPROTEIN; PARTICLES; NETWORKS;
D O I
10.1016/j.cbpa.2019.11.002
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-protein interactions play a critical role in post-transcriptional gene regulation. Characterizing these interactions in their native context has been challenging; however, advances in RNA sequencing and mass spectrometrybased proteomics combined with innovative chemical biological tools have heralded the development of robust strategies for performing biochemistry on a cellular scale. Herein, we review recent advances in the development and application of proteomic and transcriptomic approaches to profile cellular RNA-protein interactions, focusing on sequencing-based strategies and proteomic analysis of RNA-binding proteins, as well as approaches to address the role of RNA modifications in protein-RNA binding events.
引用
收藏
页码:37 / 44
页数:8
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