Huber P W, Wool I G
Proc Natl Acad Sci U S A. 1984 Jan;81(2):322-6. doi: 10.1073/pnas.81.2.322.
A rapid and convenient method has been devised to determine the binding sites for proteins on RNA. The procedure is an adaptation of one used to map DNA-protein complexes by protection against nuclease digestion. The method uses the cytotoxic ribonuclease alpha-sarcin, which hydrolyzes purines in both single- and double-stranded regions of RNA. It has been authenticated by confirming the binding sites for the Escherichia coli ribosomal proteins L18 and L25 on 5S rRNA and its value has been established by identifying the attachment site for protein L5. The procedure should be useful for the analysis of other ribonucleoprotein complexes.
已设计出一种快速便捷的方法来确定蛋白质在RNA上的结合位点。该程序是一种用于通过防止核酸酶消化来绘制DNA-蛋白质复合物图谱的方法的改编。该方法使用细胞毒性核糖核酸酶α-肌动蛋白,它能水解RNA单链和双链区域中的嘌呤。通过确认大肠杆菌核糖体蛋白L18和L25在5S rRNA上的结合位点对其进行了验证,并通过鉴定蛋白L5的附着位点确定了其价值。该程序对分析其他核糖核蛋白复合物应该是有用的。