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Why Is a High Temperature Needed by Thermus thermophilus Argonaute During mRNA Silencing: A Theoretical Study

机译:为什么嗜热栖热菌Argonaute在mRNA沉默期间需要高温:理论研究

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Thermus thermophiles Argonaute (TtAgo) is a complex, which is consisted of 5′-phosphorylated guide DNA and a series of target DNA with catalytic activities at high temperatures. To understand why high temperatures are needed for the catalytic activities, three molecular dynamics simulations and binding free energy calculations at 310, 324 and 338K were performed for the TtAgo-DNA complex to explore the conformational changes between 16-mer guide DNA/15-mer target DNA and TtAgo at different temperatures. The simulation results indicate that a collapse of a small β-strand (residues 507– 509) at 310 K caused Glu512 to move away from the catalytic residues Asp546 and Asp478, resulting in a decrease in catalytic activity, which was not observed in the simulations at 324 and 338 K. The nucleic acid binding channel became enlarged at 324 and 338K, thereby facilitating the DNA to slide in. Binding free energy calculations and hydrogen bond occupancy indicated that the interaction between TtAgo and the DNA was more stable at 324K and 338K than at 310 K. The DNA binding pocket residues Lys575 and Asn590 became less solvent accessible at 324 and 338K than at 310 K to influence hydrophilic interaction with DNA. Our simulation studies shed some light on the mechanism of TtAgo and explained why a high temperature was needed by TtAgo during gene editing of CRISPR.
机译:嗜热栖热菌Argonaute(TtAgo)是一种复合物,由5'-磷酸化的指导DNA和一系列在高温下具有催化活性的靶DNA组成。为了理解为什么高温需要催化活性,对TtAgo-DNA复合物进行了310、324和338K的三个分子动力学模拟和结合自由能计算,以探索16-mer指导DNA / 15-mer之间的构象变化在不同温度下靶向DNA和TtAgo。模拟结果表明,小的β链(残基507-509)在310 K处的塌陷导致Glu512从催化残基Asp546和Asp478移开,导致催化活性下降,这在模拟中未观察到。核酸结合通道在324和338 K时变大。从而促进DNA滑入。结合自由能计算和氢键占有率表明TtAgo和DNA之间的相互作用在324K和338K时更稳定。与310 K相比,DNA结合口袋残基Lys575和Asn590在324和338K时变得比在310 K时更少的溶剂可及性,从而影响与DNA的亲水相互作用。我们的模拟研究为TtAgo的机理提供了一些启示,并解释了为什么在CRISPR基因编辑过程中TtAgo需要高温。

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