首页> 美国卫生研究院文献>Nucleic Acids Research >RNA-protein cross-linking in Eschericia coli 30S ribosomal subunits: a method for the direct analysis of the RNA regions involved in the cross-links.
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RNA-protein cross-linking in Eschericia coli 30S ribosomal subunits: a method for the direct analysis of the RNA regions involved in the cross-links.

机译:大肠杆菌30S核糖体亚基中的RNA-蛋白质交联:直接分析参与交联的RNA区域的方法。

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摘要

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.
机译:对涉及RNA-蛋白质交联的核糖体亚基进行地形学研究的前提是,应确定RNA上的交联位点。提出了使用该30S亚基作为测试系统来解决该问题的方法,其中蛋白质S7已通过紫外线照射与16S RNA交联。该方法基于在非离子去污剂存在下的凝胶分离系统。当将包含RNA-蛋白质交联的核糖核蛋白片段应用于该系统时,非交联的蛋白质被去除,同时交联的RNA-蛋白质复合物与非交联的RNA分离。以这种方式分离的S7-RNA复合物的寡核苷酸分析表明,它由来自16S RNA的P-A部分的RNA区域组成。该区域不存在单个特征性寡核苷酸,并且初步得出结论,该缺失的寡核苷酸包含实际的交联位点。

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