Beuth Barbara, García-Mayoral María Flor, Taylor Ian A, Ramos Andres
Division of Molecular Structure, National Institute for Medical Research, The Ridgeway, Mill Hill, London NW7 1AA, U.K.
J Am Chem Soc. 2007 Aug 22;129(33):10205-10. doi: 10.1021/ja072365q. Epub 2007 Jul 26.
We describe a method to analyze the sequence specificity of an RNA-binding domain. The method, which we have named scaffold-independent analysis, reports on the specificity for each nucleotide position within an RNA target, uncoupled from the surrounding structural and sequence context. We expect this information to improve our understanding of protein-RNA interfaces in ssRNA binding domains (e.g., KH or RRM domains) and to be useful to the design of novel protein-RNA recognition surfaces. Our NMR binding assays using the third KH domain of the Nova-1 protein provide a proof-of-principle for the method and novel information on the specificity of this domain for its RNA targets.
我们描述了一种分析RNA结合结构域序列特异性的方法。我们将该方法命名为支架无关分析,它报告RNA靶标中每个核苷酸位置的特异性,而不受周围结构和序列背景的影响。我们期望这些信息能增进我们对单链RNA结合结构域(如KH或RRM结构域)中蛋白质-RNA界面的理解,并有助于设计新型蛋白质-RNA识别表面。我们使用Nova-1蛋白的第三个KH结构域进行的核磁共振结合试验为该方法提供了原理验证,并提供了有关该结构域对其RNA靶标的特异性的新信息。