Suppr超能文献

对DNA聚合酶δ精确复制DNA机制的深入了解。

Insights into DNA polymerase δ's mechanism for accurate DNA replication.

作者信息

Foley M C, Couto L, Rauf S, Boyke A

机构信息

Department of Chemistry, New Jersey City University, 2039 Kennedy Blvd., Jersey City, NJ, 07305, USA.

Department of Science, Garden City High School, 170 Rockaway Ave., Garden City, NY, 11530, USA.

出版信息

J Mol Model. 2019 Feb 27;25(3):80. doi: 10.1007/s00894-019-3957-z.

Abstract

Our study examines the mechanisms by which DNA polymerase (pol) δ faithfully replicates DNA. To better understand this process, we have performed all-atom molecular dynamics simulations of several DNA pol δ systems to identify conformational changes occurring prior to chemistry and investigate mechanisms by which mutations in the fingers domain (R696W and A699Q) lower fidelity. Our results indicate that, without the incoming nucleotide, a distinct open conformation occurs defined by a rotation in the fingers. The closed form, adopted when the correct nucleotide is bound, appears best organized for chemistry when three magnesium ions coordinate protein and DNA residues in the active site. Removing an unusual third metal ion from the polymerase active site causes shifting in the fingers and thumb as well as stimulating specific exonuclease β-hairpin-DNA interactions that fray the primer terminus base pair. These changes suggest that dissociation of the third divalent ion (metal ion 'C') signals a transfer of the DNA primer from the polymerase to the exonuclease active site and implies a role for the β-hairpin in DNA switching. Analysis of β-hairpin movement in several systems reveals a dependence on active-site changes and suggests how Lys444 and Tyr446 present in the β-hairpin can affect proofreading. Analysis of A699Q and R696W pol δ mutant systems reveal marked differences in the open-to-closed transition as well as β-hairpin repositioning that explain reduced nucleotide selectivity and higher error rates.

摘要

我们的研究考察了DNA聚合酶(pol)δ精确复制DNA的机制。为了更好地理解这一过程,我们对多个DNA pol δ系统进行了全原子分子动力学模拟,以确定化学反应之前发生的构象变化,并研究手指结构域中的突变(R696W和A699Q)降低保真度的机制。我们的结果表明,在没有即将进入的核苷酸的情况下,手指结构域的旋转会导致一种独特的开放构象。当结合正确的核苷酸时所采用的闭合形式,在三个镁离子协调活性位点中的蛋白质和DNA残基时,似乎最有利于化学反应。从聚合酶活性位点去除一个异常的第三个金属离子会导致手指和拇指结构域发生位移,并刺激特定的核酸外切酶β-发夹-DNA相互作用,从而使引物末端碱基对解链。这些变化表明,第三个二价离子(金属离子“C))的解离标志着DNA引物从聚合酶转移到核酸外切酶活性位点,并暗示了β-发夹在DNA转换中的作用。对多个系统中β-发夹运动的分析揭示了其对活性位点变化的依赖性,并表明β-发夹中存在的赖氨酸444和酪氨酸446如何影响校对。对A699Q和R696W pol δ突变体系统的分析揭示了开放到闭合转变以及β-发夹重新定位方面的显著差异,这些差异解释了核苷酸选择性降低和错误率升高的原因。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验