Bell Thomas J, Eiríksdóttir Emelía, Langel Ulo, Eberwine James
Department of Pharmacology and Psychiatry, University of Pennsylvania Medical Center, Philadelphia, PA, USA.
Methods Mol Biol. 2011;683:473-86. doi: 10.1007/978-1-60761-919-2_34.
RNA-binding proteins (RBPs) are fundamental regulatory proteins for all forms of transcriptional and posttranscriptional control of gene expression. However, isolating RBPs is technically challenging for investigators. Currently, the most widely used techniques to isolate RBPs are in vitro biochemical approaches. Although these approaches have been useful, they have several limitations. One key limitation to using in vitro biochemical approaches is that RBP-RNA interactions are isolated under nonbiological conditions. Here we review a novel experimental approach to identify RBPs called peptide nucleic acid (PNA)-assisted identification of RBPs (PAIR) technology (Zielinski et al., Proc Natl Acad Sci USA 103:1557-1562, 2006). This technology has two significant advantages over traditional approaches. (1) It overcomes the in vitro limitation of biochemical approaches by allowing investigators to isolate RBP-RNA interactions under in vivo conditions. (2) This technology is highly mRNA specific; it isolates RBPs in an exon-specific manner. By selectively targeting alternatively spliced exons with PAIR technology, investigators can isolate splice variant-specific and mRNA region-specific (5-UTR and 3-UTR) RBP complexes for any mRNA of interest.
RNA结合蛋白(RBPs)是基因表达的所有转录和转录后调控形式的基本调节蛋白。然而,对于研究人员来说,分离RBPs在技术上具有挑战性。目前,分离RBPs最广泛使用的技术是体外生化方法。尽管这些方法很有用,但它们有几个局限性。使用体外生化方法的一个关键局限性是RBP-RNA相互作用是在非生物条件下分离的。在这里,我们综述一种鉴定RBPs的新实验方法,称为肽核酸(PNA)辅助的RBPs鉴定(PAIR)技术(齐林斯基等人,《美国国家科学院院刊》103:1557 - 1562,2006)。与传统方法相比,该技术有两个显著优点。(1)它通过允许研究人员在体内条件下分离RBP-RNA相互作用,克服了生化方法的体外局限性。(2)该技术具有高度的mRNA特异性;它以外显子特异性方式分离RBPs。通过用PAIR技术选择性靶向可变剪接外显子,研究人员可以为任何感兴趣的mRNA分离剪接变体特异性和mRNA区域特异性(5'-UTR和3'-UTR)的RBP复合物。