嗜热热菌Argonaute在辅助位点的靶识别机制。

IF 2.9 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Biochemistry Biochemistry Pub Date : 2025-05-20 Epub Date: 2025-05-09 DOI:10.1021/acs.biochem.5c00056
Kun Xi, Jinchu Liu, Wenzhuo Ma, Lizhe Zhu
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引用次数: 0

摘要

嗜热热菌Argonaute (TtAgo)利用一条引导DNA链来切割外源DNA,保护细菌免受侵入性遗传元素的侵害,从而提供了作为基因编辑工具的潜力。然而,目标识别的潜在机制仍未得到充分探讨。例如,靶切割的补充位点(位置g13-16)上导靶互补的必要性已经争论多年。在这里,利用原子分子动力学模拟生成的多个转变途径,我们确定了这一过程的三个阶段:尾部释放、碱基配对和最终细化。尾部释放导致引导DNA (gDNA)完全暴露于溶剂中,从而定位gDNA和靶DNA (tDNA)之间的碱基配对作为驱动识别的主要力量。因此,所有速率决定步骤都位于碱基配对阶段。详细的研究表明,核碱基之间的π-π堆积,碱基的挤压和不匹配显著影响这些限速阶段。我们的研究结果还表明,在补充位点上,碱基位错比π-π堆叠对tDNA识别的破坏性更小。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Target Recognition Mechanism of Thermus thermophilus Argonaute at the Supplementary Site.

Thermus thermophilus Argonaute (TtAgo) utilizes a guide DNA strand to cleave foreign DNA, defending the bacteria against invasive genetic elements and thus offering potential as a gene-editing tool. However, the underlying mechanism for target recognition remains underexplored. For example, the necessity of guide-target complementarity at the supplementary site (positions g13-16) for target cleavage has been debated for years. Here, using multiple transition pathways generated by atomistic molecular dynamics simulations, we identified three stages in this process: tail release, base pairing, and final refinement. The tail release leads to full exposure of the guide DNA (gDNA) to solvents, thereby positioning base-pairing between gDNA and target DNA (tDNA) as the principal force driving recognition. Consequently, all rate-determining steps are situated within the base-pairing stage. Detailed examination indicates that π-π stacking between the nucleobases, the extrusion of bases, and mismatches significantly influence these rate-limiting stages. Our results also suggest that base dislocations are less disruptive factors than π-π stacking for tDNA recognition in the supplementary site.

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来源期刊
Biochemistry Biochemistry
Biochemistry Biochemistry 生物-生化与分子生物学
CiteScore
5.50
自引率
3.40%
发文量
336
审稿时长
1-2 weeks
期刊介绍: Biochemistry provides an international forum for publishing exceptional, rigorous, high-impact research across all of biological chemistry. This broad scope includes studies on the chemical, physical, mechanistic, and/or structural basis of biological or cell function, and encompasses the fields of chemical biology, synthetic biology, disease biology, cell biology, nucleic acid biology, neuroscience, structural biology, and biophysics. In addition to traditional Research Articles, Biochemistry also publishes Communications, Viewpoints, and Perspectives, as well as From the Bench articles that report new methods of particular interest to the biological chemistry community.
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