Xi Kun, Liu Jinchu, Ma Wenzhuo, Zhu Lizhe
School of Medicine and Warshel Institute for Computational Biology, The Chinese University of Hong Kong - Shenzhen, Shenzhen, Guangdong 518172, P. R. China.
Department of Biophysics and Department of Pathology of Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou 310058, China.
Biochemistry. 2025 May 20;64(10):2181-2191. doi: 10.1021/acs.biochem.5c00056. Epub 2025 May 9.
Argonaute (Ago) 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.
Argonaute(Ago)利用一条引导DNA链切割外源DNA,保护细菌免受入侵遗传元件的影响,因此具有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索。例如,多年来,对于在辅助位点(位置g13 - 16)处引导序列与目标序列互补性对于目标切割的必要性一直存在争议。在这里,我们利用原子分子动力学模拟生成的多个过渡途径,确定了这个过程中的三个阶段:尾部释放、碱基配对和最终优化。尾部释放导致引导DNA(gDNA)完全暴露于溶剂中,从而使gDNA与目标DNA(tDNA)之间的碱基配对成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。详细研究表明,核碱基之间的π-π堆积、碱基的挤出以及错配显著影响这些限速阶段。我们的结果还表明,对于辅助位点中tDNA的识别,碱基错位比π-π堆积的干扰因素要小。