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用于大肠杆菌内部核糖体结构的光不稳定寡聚脱氧核糖核酸探针。

Photolabile oligoDNA probes of internal Escherichia coli ribosomal structure.

作者信息

Cooperman B S, Alexander R W, Muralikrishna P

机构信息

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

出版信息

Nucleic Acids Symp Ser. 1995(33):59-62.

PMID:8643399
Abstract

We are examining the spatial arrangement of ribosomal components in the vicinity of rRNA sequences of particular significance for ribosome structure and function through the use of radioactive, photolabile derivatives of oligoDNAs complementary to such sequences. The oligoDNA probes bind to their target sequences in intact ribosomal subunits, and, on photolysis, incorporate into neighboring ribosomal components. Labeled ribosomal proteins are subsequently identified by SDS-PAGE, RP-HPLC and immunoprecipitation. Labeled rRNA is identified at the nucleotide level by RNase H cleavage and primer extension. The results obtained provide a description of the neighborhood surrounding a particular rRNA sequence and impose important constraints on the evolving three-dimensional models of both the 30S and 50S subunits, since they typically oblige several ribosomal components to fall within defined distances of the targeted rRNA. Our results will be discussed in terms of these models, emphasizing their consistency or inconsistency.

摘要

我们正在通过使用与特定序列互补的寡脱氧核糖核酸(oligoDNA)的放射性、光不稳定衍生物,来研究核糖体组分在对核糖体结构和功能具有特别重要意义的rRNA序列附近的空间排列。寡脱氧核糖核酸探针与完整核糖体亚基中的靶序列结合,并且在光解后,整合到相邻的核糖体组分中。随后通过SDS-PAGE、反相高效液相色谱(RP-HPLC)和免疫沉淀鉴定标记的核糖体蛋白。通过核糖核酸酶H切割和引物延伸在核苷酸水平鉴定标记的rRNA。所获得的结果描述了特定rRNA序列周围的邻域,并对30S和50S亚基不断发展的三维模型施加了重要限制,因为它们通常要求几个核糖体组分落在靶向rRNA的限定距离内。我们将根据这些模型讨论我们的结果,强调它们的一致性或不一致性。

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