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DNA/RNA 聚合酶催化的核酸聚合的自激活机制。

A Self-Activated Mechanism for Nucleic Acid Polymerization Catalyzed by DNA/RNA Polymerases.

机构信息

Laboratory of Molecular Modeling & Drug Discovery, Istituto Italiano di Tecnologia , Via Morego 30, 16163, Genoa, Italy.

IAS-5/INM-9 Computational Biomedicine and JARA-HPC, Forschungszentrum Jülich , Wilhelm-Johnen-Strasse, 52428 Jülich, Germany.

出版信息

J Am Chem Soc. 2016 Nov 9;138(44):14592-14598. doi: 10.1021/jacs.6b05475. Epub 2016 Aug 31.

Abstract

The enzymatic polymerization of DNA and RNA is the basis for genetic inheritance for all living organisms. It is catalyzed by the DNA/RNA polymerase (Pol) superfamily. Here, bioinformatics analysis reveals that the incoming nucleotide substrate always forms an H-bond between its 3'-OH and β-phosphate moieties upon formation of the Michaelis complex. This previously unrecognized H-bond implies a novel self-activated mechanism (SAM), which synergistically connects the in situ nucleophile formation with subsequent nucleotide addition and, importantly, nucleic acid translocation. Thus, SAM allows an elegant and efficient closed-loop sequence of chemical and physical steps for Pol catalysis. This is markedly different from previous mechanistic hypotheses. Our proposed mechanism is corroborated via ab initio QM/MM simulations on a specific Pol, the human DNA polymerase-η, an enzyme involved in repairing damaged DNA. The structural conservation of DNA and RNA Pols supports the possible extension of SAM to Pol enzymes from the three domains of life.

摘要

DNA 和 RNA 的酶促聚合是所有生物遗传的基础。它由 DNA/RNA 聚合酶 (Pol) 超家族催化。在这里,生物信息学分析表明,在形成 Michaelis 复合物时,进入的核苷酸底物总是在其 3'-OH 和 β-磷酸部分之间形成氢键。这种以前未被识别的氢键意味着一种新的自我激活机制 (SAM),它协同连接原位亲核形成与随后的核苷酸添加,重要的是,核酸易位。因此,SAM 允许 Pol 催化的化学和物理步骤的优雅和高效的闭环序列。这与以前的机械假设明显不同。我们提出的机制通过对特定 Pol(参与修复受损 DNA 的人 DNA 聚合酶 - η)的从头 ab initio QM/MM 模拟得到了证实。DNA 和 RNA Pol 的结构保守性支持 SAM 可能扩展到来自生命三个领域的 Pol 酶。

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