Zwieb C, Brimacombe R
Nucleic Acids Res. 1978 Apr;5(4):1189-206. doi: 10.1093/nar/5.4.1189.
A prerequisite for topographical studies on ribosomal subunits involving RNA-protein cross-linking is that the cross-linking sites on the RNA should be determined. Methodology is presented which offers a solution to this problem, using as a test system 30S subunits in which protein S7 has been cross-linked to the 16S RNA by ultraviolet irradiation. The method is based on a gel separation system in the presence of a non-ionic detergent. When a ribonucleoprotein fragment containing RNA-protein cross-links is applied to this system, non-cross-linked protein is removed, and simultaneously the cross-linked RNA-protein complex is separated from non-cross-linked RNA. Oligonucleotide analysis of the S7-RNA complex isolated in this manner showed it to consist of a region of RNA from sections P-A of the 16S RNA. A single characteristic oligonucleotide was absent from this region, and it was tentatively concluded that this missing oligonucleotide contains the actual site of cross-linking.
进行涉及RNA-蛋白质交联的核糖体亚基拓扑学研究的一个前提条件是确定RNA上的交联位点。本文介绍了一种解决该问题的方法,使用经紫外线照射使蛋白质S7与16S RNA交联的30S亚基作为测试系统。该方法基于在非离子去污剂存在下的凝胶分离系统。当将含有RNA-蛋白质交联的核糖核蛋白片段应用于该系统时,非交联蛋白被去除,同时交联的RNA-蛋白质复合物与非交联RNA分离。对以这种方式分离的S7-RNA复合物进行的寡核苷酸分析表明,它由16S RNA中P-A节段的一个RNA区域组成。该区域缺少一个单一的特征性寡核苷酸,并初步得出结论,这个缺失的寡核苷酸包含实际的交联位点。