Ma Wenzhuo, Lyu Wenping, Zhu Lizhe
School of Medicine, Warshel Institute for Computational Biology, The Chinese University of Hong Kong-Shenzhen, Shenzhen 518172, China.
Int J Mol Sci. 2025 May 15;26(10):4738. doi: 10.3390/ijms26104738.
Argonaute (Ago) can achieve DNA-guided DNA recognition and cleavage at physiological temperatures (~37 °C), making it a promising tool for gene editing. However, its significant off-target effects, particularly associated with the seed region (sites 2-8), pose challenges for precise gene therapy. This study focuses on enhancing the specificity of the seed region recognition to mitigate these off-target effects. We investigated the molecular recognition process between the Ago-gDNA complex and the seed region of the target DNA using molecular dynamics simulations and automated path searching. Our findings reveal that positively charged residues located in an α-helix domain at the DNA-protein interface (R279, H285, K287, K288, K291, K298) facilitate rapid binding to the DNA phosphate backbone. Such interaction enhances the pre-formation of the DNA double helix, reducing the reliance on base complementarity during duplex pairing. Further simulations showed that alanine replacement of these positively charged residues led to significantly improved sequence specificity for the target DNA seed region. Collectively, these results offered critical insights into the origin of off-target recognition by Ago in its seed region, shedding lights on its fidelity enhancement.
阿贡纳特蛋白(Ago)能够在生理温度(约37°C)下实现DNA引导的DNA识别和切割,使其成为一种很有前景的基因编辑工具。然而,其显著的脱靶效应,尤其是与种子区域(第2至8位)相关的脱靶效应,给精确基因治疗带来了挑战。本研究着重于提高种子区域识别的特异性,以减轻这些脱靶效应。我们使用分子动力学模拟和自动路径搜索研究了Ago-gDNA复合物与靶DNA种子区域之间的分子识别过程。我们的研究结果表明,位于DNA-蛋白质界面α-螺旋结构域中的带正电荷残基(R279、H285、K287、K288、K291、K298)有助于快速结合到DNA磷酸骨架上。这种相互作用增强了DNA双螺旋的预形成,减少了双链配对过程中对碱基互补性的依赖。进一步的模拟表明,将这些带正电荷的残基替换为丙氨酸可显著提高对靶DNA种子区域的序列特异性。总的来说,这些结果为Ago在其种子区域的脱靶识别起源提供了关键见解,为提高其保真度提供了思路。