European Molecular Biology Laboratory, Heidelberg, Germany.
Cell. 2012 Jun 8;149(6):1393-406. doi: 10.1016/j.cell.2012.04.031. Epub 2012 May 31.
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.
RNA 结合蛋白 (RBPs) 从合成到降解决定了 RNA 的命运。我们采用了两种互补的方法来实现 RBPs 与 RNA 的共价 UV 交联,从而描述了一种系统的、无偏的、全面的方法,称为“相互作用组捕获”,用于定义增殖的人 HeLa 细胞的 mRNA 相互作用组。我们通过生化和统计标准鉴定了 860 种符合 RBP 标准的蛋白质,为之前已知的 RBP 增加了 300 多种,并揭示了疾病中的 RBP、中间代谢的 RNA 结合酶、RNA 结合激酶和 RNA 结合结构。出乎意料的是,我们发现 HeLa mRNA 相互作用组中的许多蛋白质高度无序,富含短重复氨基酸基序。相互作用组捕获广泛适用于研究不同生物学环境中 mRNA 相互作用组的组成和动态变化。