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一种铅依赖型核酶的晶体结构揭示了与催化相关的金属结合位点。

Crystal structure of a lead-dependent ribozyme revealing metal binding sites relevant to catalysis.

作者信息

Wedekind J E, McKay D B

机构信息

Department of Structural Biology, Stanford University School of Medicine, California 94305-5126, USA.

出版信息

Nat Struct Biol. 1999 Mar;6(3):261-8. doi: 10.1038/6700.

Abstract

The leadzyme is a small RNA motif that catalyzes a site-specific, Pb2+-dependent cleavage reaction. As such, it is an example of a metal-dependent RNA enzyme. Here we describe the X-ray crystallographic structure of the leadzyme, which reveals two independent molecules per asymmetric unit. Both molecules feature an internal loop in which a bulged purine base stack twists away from the helical stem. This kinks the backbone, rendering the phosphodiester bond susceptible to cleavage. The independent molecules have different conformations: one leadzyme copy coordinates Mg2+, whereas the other binds only Ba2+ or Pb2+. In the active site of the latter molecule, a single Ba2+ ion coordinates the 2'-OH nucleophile, and appears to mimic the binding of catalytic lead. These observations allow a bond cleavage reaction to be modeled, which reveals the minimal structural features necessary for catalysis by this small ribozyme.

摘要

引导酶是一种小RNA基序,可催化位点特异性、Pb2+依赖性切割反应。因此,它是金属依赖性RNA酶的一个例子。在这里,我们描述了引导酶的X射线晶体结构,该结构揭示了每个不对称单元有两个独立的分子。两个分子都有一个内环,其中一个凸起的嘌呤碱基堆积从螺旋茎扭转开。这使主链发生扭结,使磷酸二酯键易于切割。独立的分子具有不同的构象:一个引导酶拷贝与Mg2+配位,而另一个仅结合Ba2+或Pb2+。在后者分子的活性位点,单个Ba2+离子与2'-OH亲核试剂配位,似乎模拟了催化铅的结合。这些观察结果使我们能够对键切割反应进行建模,揭示了这种小核酶催化所需的最小结构特征。

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