Zang Shangbing, Lin Ren-Jang
Department of Molecular and Cellular Biology, Beckman Research Institute of the City of Hope, 1500 E. Duarte Road, Duarte, CA, 91010, USA.
Irell & Manella Graduate School of Biological Sciences of the City of Hope, Duarte, CA, USA.
Methods Mol Biol. 2016;1421:111-25. doi: 10.1007/978-1-4939-3591-8_10.
Northwestern assays detect a direct binding of a given RNA molecule to a protein immobilized on a nitrocellulose membrane. Here, we describe protocols to prepare (32)P-labeled RNA probes and to use them to assay for RNA-protein interactions after partially purified protein preparations are resolved on denaturing SDS-polyacrylamide gels. The method can unambiguously determine whether the protein of interest can directly and independently bind RNA even in the presence of contaminating bacterial proteins or degradation products that at times may hinder interpretation of results obtained from gel mobility shift or RNP immunoprecipitation assays.
蛋白质印迹法可检测特定RNA分子与固定在硝酸纤维素膜上的蛋白质之间的直接结合。在此,我们描述了制备(32)P标记RNA探针的方法,以及在变性SDS-聚丙烯酰胺凝胶上分离部分纯化的蛋白质制剂后,使用这些探针检测RNA-蛋白质相互作用的方法。即使存在有时可能会妨碍从凝胶迁移率变动或RNP免疫沉淀分析中获得的结果解释的污染细菌蛋白质或降解产物,该方法也能明确确定感兴趣的蛋白质是否能直接且独立地结合RNA。