Wower I, Brimacombe R
Nucleic Acids Res. 1983 Mar 11;11(5):1419-37. doi: 10.1093/nar/11.5.1419.
RNA-protein cross-links were introduced into E. coli 30S ribosomal subunits by reaction with 2-iminothiolane followed by a mild ultraviolet irradiation treatment. After removal of non-reacted protein and partial nuclease digestion of the cross-linked 16S RNA-protein moiety, a number of individual cross-linked complexes could be isolated and the sites of attachment of the proteins to the RNA determined. Protein S8 was cross-linked to the RNA at three different positions, within oligo-nucleotides encompassing positions 629-633, 651-654, and (tentatively) 593-597 in the 16S sequence. Protein S7 was cross-linked within two oligonucleotides encompassing positions 1238-1240, and 1377-1378. In addition, a site at position 723-724 was observed, cross-linked to protein S19, S20 or S21.
通过与2-亚氨基硫杂环戊烷反应,随后进行温和的紫外线照射处理,将RNA-蛋白质交联引入大肠杆菌30S核糖体亚基。去除未反应的蛋白质并对交联的16S RNA-蛋白质部分进行部分核酸酶消化后,可以分离出许多单独的交联复合物,并确定蛋白质与RNA的附着位点。蛋白质S8在16S序列中包含629-633、651-654和(暂定)593-597位置的寡核苷酸内的三个不同位置与RNA交联。蛋白质S7在包含1238-1240和1377-1378位置的两个寡核苷酸内交联。此外,在723-724位置观察到一个位点,与蛋白质S19、S20或S21交联。