相互作用体
生物
RNA结合蛋白
核糖核酸
信使核糖核酸
细胞生物学
计算生物学
基因
遗传学
作者
Alfredo Castelló,Bernd Fischer,Katrin Eichelbaum,Rastislav Horos,Benedikt M. Beckmann,Claudia Strein,Norman E. Davey,David T. Humphreys,Thomas Preiß,Lars M. Steinmetz,Jeroen Krijgsveld,Matthias W. Hentze
出处
期刊:Cell
[Elsevier]
日期:2012-06-01
卷期号:149 (6): 1393-1406
被引量:1767
标识
DOI:10.1016/j.cell.2012.04.031
摘要
RNA-binding proteins (RBPs) determine RNA fate from synthesis to decay. Employing two complementary protocols for covalent UV crosslinking of RBPs to RNA, we describe a systematic, unbiased, and comprehensive approach, termed "interactome capture," to define the mRNA interactome of proliferating human HeLa cells. We identify 860 proteins that qualify as RBPs by biochemical and statistical criteria, adding more than 300 RBPs to those previously known and shedding light on RBPs in disease, RNA-binding enzymes of intermediary metabolism, RNA-binding kinases, and RNA-binding architectures. Unexpectedly, we find that many proteins of the HeLa mRNA interactome are highly intrinsically disordered and enriched in short repetitive amino acid motifs. Interactome capture is broadly applicable to study mRNA interactome composition and dynamics in varied biological settings.
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