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Accurate placement of substrate RNA by Gar1 in H/ACA RNA-guided pseudouridylation

机译:Gar1在H / ACA RNA引导的伪尿中精确定位底物RNA

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摘要

H/ACA RNA-guided ribonucleoprotein particle (RNP), the most complicated RNA pseudouridylase so far known, uses H/ACA guide RNA for substrate capture and four proteins (Cbf5, Nop10, L7Ae and Gar1) for pseudouridylation. Although it was shown that Gar1 not only facilitates the product release, but also enhances the catalytic activity, the chemical role that Gar1 plays in this complicated machinery is largely unknown. Kinetics measurement on italic toggle="yes">Pyrococcus furiosus RNPs at different temperatures making use of fluorescence anisotropy showed that Gar1 reduces the catalytic barrier through affecting the activation entropy instead of enthalpy. Site-directed mutagenesis combined with molecular dynamics simulations demonstrated that V149 in the thumb loop of Cbf5 is critical in placing the target uridine to the right position toward catalytic D85 of Cbf5. The enzyme elegantly aligns the position of uridine in the catalytic site with the help of Gar1. In addition, conversion of uridine to pseudouridine results in a rigid syn configuration of the target nucleotide in the active site and causes Gar1 to pull out the thumb. Both factors guarantee the efficient release of the product.
机译:H / ACA RNA引导的核糖核蛋白颗粒(RNP)是迄今为止最复杂的RNA伪尿苷酸酶,它使用H / ACA引导RNA进行底物捕获,并使用四种蛋白质(Cbf5,Nop10,L7Ae和Gar1)进行伪尿苷化。尽管已显示Gar1不仅有助于产物释放,而且还增强了催化活性,但很大程度上未知Gar1在这种复杂机械中所起的化学作用。利用荧光各向异性在不同温度下对激烈热球菌RNPs的动力学测量表明,Gar1通过影响活化熵而不是焓来减少催化屏障。定点诱变与分子动力学模拟相结合表明,Cbf5拇指环中的V149对于将目标尿苷置于Cbf5的催化D85的正确位置至关重要。该酶借助Gar1优雅地将尿苷在催化位点上对齐。另外,尿苷向伪尿苷的转化导致活性位点中靶核苷酸的刚性syn构型,并使Gar1伸出拇指。这两个因素都保证了产品的有效释放。

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