Muralikrishna P, Cooperman B S
Department of Chemistry, University of Pennsylvania, Philadelphia 19104-6323.
Biochemistry. 1995 Jan 10;34(1):115-21. doi: 10.1021/bi00001a014.
We report the synthesis of a radioactive, photolabile oligodeoxyribonucleotide probe and its exploitation in identifying 50S ribosomal subunit components neighboring its target site in 23S rRNA. The probe is complementary to 23S rRNA nucleotides 2475-2483, a single-stranded sequence (the 2475 loop) near the peptidyltransferase center of Escherichia coli ribosomes. On photolysis in the presence of 50S subunits, it site-specifically incorporates into proteins L1, L13, L16, L32, and L33 and into 23S rRNA nucleotides G2470, A2471, and G2472. These results provide clear evidence that C2475 in 23S rRNA is within 21 A (the distance between C2475 and the photogenerated nitrene) of proteins L1, L13, L16, L32, and L33. The implications of these results for the evolving model of the internal structure of the 50S subunit are considered.
我们报告了一种放射性、光不稳定的寡脱氧核糖核苷酸探针的合成及其在鉴定23S rRNA中与其靶位点相邻的50S核糖体亚基成分中的应用。该探针与23S rRNA的核苷酸2475 - 2483互补,这是大肠杆菌核糖体肽基转移酶中心附近的一个单链序列(2475环)。在50S亚基存在下进行光解时,它位点特异性地掺入蛋白质L1、L13、L16、L32和L33以及23S rRNA的核苷酸G2470、A2471和G2472中。这些结果提供了明确的证据,表明23S rRNA中的C2475位于蛋白质L1、L13、L16、L32和L33的21埃范围内(C2475与光生成的氮烯之间的距离)。我们考虑了这些结果对50S亚基内部结构不断发展的模型的影响。