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丁型肝炎病毒核酶的晶体结构。

Crystal structure of a hepatitis delta virus ribozyme.

作者信息

Ferré-D'Amaré A R, Zhou K, Doudna J A

机构信息

Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut 06520-8114, USA.

出版信息

Nature. 1998 Oct 8;395(6702):567-74. doi: 10.1038/26912.

Abstract

The self-cleaving ribozyme of the hepatitis delta virus (HDV) is the only catalytic RNA known to be required for the viability of a human pathogen. We obtained crystals of a 72-nucleotide, self-cleaved form of the genomic HDV ribozyme that diffract X-rays to 2.3 A resolution by engineering the RNA to bind a small, basic protein without affecting ribozyme activity. The co-crystal structure shows that the compact catalytic core comprises five helical segments connected as an intricate nested double pseudoknot. The 5'-hydroxyl leaving group resulting from the self-scission reaction is buried deep within an active-site cleft produced by juxtaposition of the helices and five strand-crossovers, and is surrounded by biochemically important backbone and base functional groups in a manner reminiscent of protein enzymes.

摘要

丁型肝炎病毒(HDV)的自我切割核酶是已知的唯一一种对人类病原体生存能力必需的催化RNA。我们通过对RNA进行工程改造,使其结合一种小的碱性蛋白而不影响核酶活性,从而获得了基因组HDV核酶72个核苷酸的自我切割形式的晶体,其X射线衍射分辨率达到2.3埃。共晶体结构表明,紧密的催化核心由五个螺旋片段组成,连接成一个复杂的嵌套双假结。自我切割反应产生的5'-羟基离去基团深埋在由螺旋和五个链交叉并列产生的活性位点裂隙中,并被具有重要生化意义的主链和碱基官能团包围,其方式让人联想到蛋白质酶。

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