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A contact photo-cross-linking investigation of the active site of the 8-17 deoxyribozyme.

机译:8-17脱氧核酶活性位点的接触光交联研究。

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摘要

The small RNA-cleaving 8-17 deoxyribozyme (DNAzyme) has been the subject of extensive mechanistic and structural investigation, including a number of recent single-molecule studies of its global folding. Little detailed insight exists, however, into this DNAzyme's active site; for instance, the identity of specific nucleotides that are proximal to or in contact with the scissile site in the substrate. Here, we report a systematic replacement of a number of bases within the magnesium-folded DNAzyme-substrate complex with thio- and halogen-substituted base analogues, which were then photochemically activated to generate contact cross-links within the complex. Mapping of the cross-links revealed a striking pattern of DNAzyme-substrate cross-links but an absence of significant intra-DNAzyme cross-links. Notably, the two nucleotides directly flanking the scissile phosphodiester cross-linked strongly with functionally important elements within the DNAzyme, the thymine of a G.T wobble base pair, a WCGR bulge loop, and a terminal AGC loop. Mutation of the wobble base pair to a G-C pair led to a significant folding instability of the DNAzyme-substrate complex. The cross-linking patterns obtained were used to generate a model for the DNAzyme's active site that had the substrate's scissile phosphodiester sandwiched between the DNAzyme's wobble thymine and its AGC and WCGR loops.
机译:小RNA切割8-17脱氧核酶(DNAzyme)已成为广泛的机制和结构研究的主题,包括有关其全球折叠性的许多近期单分子研究。然而,对该DNAzyme的活性位点了解甚少。例如,与底物中易裂位点近端或接触的特定核苷酸的身份。在这里,我们报道了镁折叠的DNAzyme-底物复合物中的许多碱基被硫和卤素取代的碱基类似物系统地取代,然后被光化学活化以在复合物中产生接触交联。交联的作图显示了DNAzyme-底物交联的惊人模式,但没有明显的DNAzyme内交联。值得注意的是,直接位于易裂磷酸二酯侧翼的两个核苷酸与DNAzyme,G.T摆动碱基对的胸腺嘧啶,WCGR凸起环和末端AGC环中的功能重要元件牢固地交联。摆动碱基对突变为G-C对导致DNAzyme-底物复合物的明显折叠不稳定性。所获得的交联模式用于生成DNAzyme活性位点的模型,该酶具有夹在DNAzyme摆动胸腺嘧啶及其AGC和WCGR环之间的底物易裂磷酸二酯。

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