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在高阶折纸纳米结构中可视化活性氧诱导的DNA损伤过程

Visualizing Reactive Oxygen Species-Induced DNA Damage Process in Higher-Ordered Origami Nanostructures.

作者信息

Zhang Shuangye, Xie Xiaodong, Zhang Hairuo, Zhao Ziwei, Xia Kai, Song Haitao, Li Qian, Li Mingqiang, Ge Zhilei

机构信息

School of Chemistry and Chemical Engineering, New Cornerstone Science Laboratory, Frontiers Science Center for Transformative Molecules, Zhangjiang Institute for Advanced Study and National Center for Translational Medicine, Shanghai Jiao Tong University, Shanghai 200240, China.

Shanghai Artificial Intelligence Research Institute, Shanghai 200240, China.

出版信息

JACS Au. 2025 Jan 23;5(2):965-974. doi: 10.1021/jacsau.4c01203. eCollection 2025 Feb 24.

Abstract

The genetic information on organisms is stored in the cell nucleus in the form of higher-ordered DNA structures. Here, we use DNA framework nanostructures (DFNs) to simulate the compaction and stacking density of nucleosome DNA for precise conformational and structure determination, particularly the dynamic structural changes, preferential reaction regions, and sites of DFNs during the reactive oxygen species (ROS) reaction process. By developing an atomic force microscopy-based single-particle analysis (SPA) data reconstruction method to collect and reanalyze imaging information, we demonstrate that the geometric morphology of DFNs constrains their reaction kinetics with ROS, where local mechanical stress and regional base distribution are two key factors affecting their kinetics. Furthermore, we plot the reaction process diagram for ROS and DFNs, showing the reaction process and intermediate products with individual activation energies. This SPA method offers new research tools and insights for studying the dynamic changes of highly folded and organized DNA structural domains within the nucleus and helps to reveal the key mechanisms behind their functional differences in topologically associating domains.

摘要

生物体的遗传信息以高阶DNA结构的形式存储在细胞核中。在此,我们使用DNA框架纳米结构(DFN)来模拟核小体DNA的压缩和堆积密度,以进行精确的构象和结构测定,特别是在活性氧(ROS)反应过程中DFN的动态结构变化、优先反应区域和位点。通过开发基于原子力显微镜的单颗粒分析(SPA)数据重建方法来收集和重新分析成像信息,我们证明DFN的几何形态限制了它们与ROS的反应动力学,其中局部机械应力和区域碱基分布是影响其动力学的两个关键因素。此外,我们绘制了ROS与DFN的反应过程图,显示了具有各自活化能的反应过程和中间产物。这种SPA方法为研究细胞核内高度折叠和有组织的DNA结构域的动态变化提供了新的研究工具和见解,并有助于揭示其在拓扑相关结构域中功能差异背后的关键机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75e1/11863157/d6aa592455fe/au4c01203_0001.jpg

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