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肽基转移酶中心的光不稳定寡脱氧核糖核苷酸探针:邻近核糖体成分的鉴定

A photolabile oligodeoxyribonucleotide probe of the peptidyltransferase center: identification of neighboring ribosomal components.

作者信息

Muralikrishna P, Cooperman B S

机构信息

Department of Chemistry, University of Pennsylvania, Philadelphia 19104-6323.

出版信息

Biochemistry. 1991 Jun 4;30(22):5421-8. doi: 10.1021/bi00236a014.

DOI:10.1021/bi00236a014
PMID:2036410
Abstract

In this work 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 2497-2505, a single-stranded sequence that has been shown to fall within the peptidyltransferase center of Escherichia coli ribosomes [Cooperman, B. S., Weitzmann, C. J., & Fernandez, C. L. (1990) in The Ribosome: Structure, Function, & Evolution (Hill, W. E., Dahlberg, A., Garrett, R. A., Moore, P. B., Schlesinger, D., & Warner, J. R., Eds.) pp 491-501, American Society of Microbiology, Washington]. On photolysis in the presence of 50S ribosomes, it site-specifically incorporates into protein L3 (identified by both SDS-PAGE and immunological methods) and into three separate 23S rRNA regions: specifically, nucleotides 2454; 2501, 2502, 2505, 2506; and 2583, 2584. These results provide clear evidence that G-2505 in 23S rRNA is within 24 A (the distance between G-2505 and the photogenerated nitrene) of protein L3 and of each of the nucleotides mentioned above and are of obvious importance in the construction of detailed three-dimensional models of ribosomal structure. The approach we present is general and can be applied to determining ribosomal components neighboring regions of rRNA that are susceptible to binding by complementary oligodeoxyribonucleotides, both in intact 30S and 50S subunits and in subunits at various stages of reconstitution.

摘要

在本研究中,我们报道了一种放射性、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核糖体亚基成分方面的应用。该探针与23S rRNA的核苷酸2497 - 2505互补,这是一个单链序列,已被证明位于大肠杆菌核糖体的肽基转移酶中心内[库珀曼,B. S.,魏茨曼,C. J.,& 费尔南德斯,C. L.(1990年),《核糖体:结构、功能与进化》(希尔,W. E.,达尔伯格,A.,加勒特,R. A.,摩尔,P. B.,施莱辛格,D.,& 华纳,J. R.编),第491 - 501页,美国微生物学会,华盛顿]。在50S核糖体存在的情况下进行光解时,它位点特异性地掺入蛋白质L3(通过SDS - PAGE和免疫学方法鉴定)以及三个独立的23S rRNA区域:具体而言,核苷酸2454;2501、2502、2505、2506;以及2583、2584。这些结果提供了明确的证据,表明23S rRNA中的G - 2505距离蛋白质L3以及上述每个核苷酸在24 Å 以内(G - 2505与光生成的氮烯之间的距离),并且在构建核糖体结构的详细三维模型中具有明显的重要性。我们提出的方法具有通用性,可应用于确定完整的30S和50S亚基以及重组不同阶段的亚基中,与易被互补寡脱氧核糖核苷酸结合的rRNA区域相邻的核糖体成分。

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A photolabile oligodeoxyribonucleotide probe of the peptidyltransferase center: identification of neighboring ribosomal components.肽基转移酶中心的光不稳定寡脱氧核糖核苷酸探针:邻近核糖体成分的鉴定
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Large-scale motions within ribosomal 50S subunits as demonstrated using photolabile oligonucleotides.使用光不稳定寡核苷酸所展示的核糖体50S亚基内的大规模运动。
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Nucleic Acids Res. 1996 Oct 15;24(20):3996-4002. doi: 10.1093/nar/24.20.3996.
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