Département de Biochimie, Université de Montréal, CP 6128, Succursale Centre-Ville, Montréal, Québec H3C 3J7, Canada.
Nucleic Acids Res. 2011 May;39(10):4427-37. doi: 10.1093/nar/gkq1244. Epub 2011 Jan 25.
The Neurospora VS ribozyme is a small nucleolytic ribozyme with unique primary, secondary and global tertiary structures, which displays mechanistic similarities to the hairpin ribozyme. Here, we determined the high-resolution NMR structure of a stem-loop VI fragment containing the A730 internal loop, which forms part of the active site. In the presence of magnesium ions, the A730 loop adopts a structure that is consistent with existing biochemical data and most likely reflects its conformation in the VS ribozyme prior to docking with the cleavage site internal loop. Interestingly, the A730 loop adopts an S-turn motif that is also present in loop B within the hairpin ribozyme active site. The S-turn appears necessary to expose the Watson-Crick edge of a catalytically important residue (A756) so that it can fulfill its role in catalysis. The A730 loop and the cleavage site loop of the VS ribozyme display structural similarities to internal loops found in the active site of the hairpin ribozyme. These similarities provided a rationale to build a model of the VS ribozyme active site based on the crystal structure of the hairpin ribozyme.
Neurospora VS 核酶是一种具有独特的一级、二级和整体三级结构的小核酶,其机制与发夹核酶相似。在这里,我们确定了含有 A730 内环的茎环 VI 片段的高分辨率 NMR 结构,该片段构成活性部位的一部分。在镁离子存在下,A730 环采用与现有生化数据一致的结构,很可能反映了它在与切割位点内环对接之前在 VS 核酶中的构象。有趣的是,A730 环采用 S 形转弯模体,该模体也存在于发夹核酶活性部位的环 B 中。S 形转弯似乎是必需的,以暴露催化重要残基(A756)的 Watson-Crick 边缘,从而使其能够在催化中发挥作用。VS 核酶的 A730 环和切割位点环与发夹核酶活性部位内环具有结构相似性。这些相似性为基于发夹核酶晶体结构构建 VS 核酶活性部位模型提供了依据。