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DSL核酶的结构与生化特性

Structural and biochemical characterization of DSL ribozyme.

作者信息

Horie Souta, Ikawa Yoshiya, Inoue Tan

机构信息

Graduate School of Biostudies, Kyoto University, Kyoto 606-8502, Japan.

出版信息

Biochem Biophys Res Commun. 2006 Jan 6;339(1):115-21. doi: 10.1016/j.bbrc.2005.11.007. Epub 2005 Nov 9.

Abstract

We recently reported on the molecular design and synthesis of a new RNA ligase ribozyme (DSL), whose active site was selected from a sequence library consisting of 30 random nucleotides set on a defined 3D structure of a designed RNA scaffold. In this study, we report on the structural and biochemical analyses of DSL. Structural analysis indicates that the active site, which consists of the selected sequence, attaches to the folded scaffold as designed. To see whether DSL resembles known ribozymes, a biochemical assay was performed. Metal-dependent kinetic studies suggest that the ligase requires Mg2+ ions. The replacement of Mg2+ with Co(NH3)6(3+) prohibits the reaction, indicating that DSL requires innersphere coordination of Mg2+ for a ligation reaction. The results show that DSL has requirements similar to those of previously reported catalytic RNAs.

摘要

我们最近报道了一种新型RNA连接酶核酶(DSL)的分子设计与合成,其活性位点是从一个由30个随机核苷酸组成的序列库中筛选出来的,该序列库设置在一个设计好的RNA支架的特定三维结构上。在本研究中,我们报道了DSL的结构和生化分析。结构分析表明,由所选序列组成的活性位点按设计附着在折叠的支架上。为了探究DSL是否类似于已知的核酶,我们进行了生化分析。金属依赖性动力学研究表明,该连接酶需要Mg2+离子。用Co(NH3)6(3+)取代Mg2+会抑制反应,这表明DSL的连接反应需要Mg2+的内球配位。结果表明,DSL的要求与先前报道的催化RNA相似。

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