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VS核酶活性位点环的溶液结构揭示了一个动态“热点”。

The solution structure of the VS ribozyme active site loop reveals a dynamic "hot-spot".

作者信息

Flinders Jeremy, Dieckmann Thorsten

机构信息

Department of Chemistry, University of California at Davis, 95616, USA.

出版信息

J Mol Biol. 2004 Aug 20;341(4):935-49. doi: 10.1016/j.jmb.2004.06.084.

Abstract

The VS ribozyme is the largest ribozyme in its class and is also the least structurally characterized thus far. The current working model of the VS ribozyme locates the active site in stem-loop VI. The solution structure of this active site loop was determined using high resolution NMR spectroscopy. The structure reveals that the ground-state conformation of the active site differs significantly from that determined previously from chemical structure probing and mutational analysis of the ribozyme in its active conformation, which contains several looped out bases. In contrast, the base-pairing scheme found for the isolated loop contains three mismatched base-pairs: an A+-C, a G-U wobble, and a sheared G-A base-pair and no looped out bases. Dynamics observed within the active site loop provide insight into the mechanism by which the RNA can rearrange its secondary structure into an "activated" conformation prior to cleavage. These findings lend support to the idea that RNA secondary structure is more fluid than once believed and that a better understanding of structure and dynamic features of ribozymes is required to unravel the intricacies of their catalytic abilities.

摘要

VS核酶是其类别中最大的核酶,也是迄今为止结构特征最少的核酶。目前关于VS核酶的工作模型将活性位点定位在茎环VI中。使用高分辨率核磁共振光谱法确定了该活性位点环的溶液结构。该结构表明,活性位点的基态构象与先前通过化学结构探测和处于活性构象的核酶的突变分析所确定的构象有显著差异,后者包含几个环出的碱基。相比之下,分离环中发现的碱基配对方案包含三个错配碱基对:一个A+-C、一个G-U摆动和一个剪切的G-A碱基对,且没有环出的碱基。在活性位点环内观察到的动力学为RNA在切割前将其二级结构重排为“活化”构象的机制提供了见解。这些发现支持了这样一种观点,即RNA二级结构比以前认为的更具流动性,并且需要更好地理解核酶的结构和动态特征,以揭示其催化能力的复杂性。

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