高性能合作 DNA 纳米器件实现灵敏的环状 RNA 成像和精确的肿瘤生长抑制

Ye Zhang, Siting Chen, Shihua Luo, Wenbin Li, Lifeng Zhang, Fei Lan, Yitong Zhu, Huijun Du, Ke Li, Chunchen Liu, Bo Situ, Bo Li, Xiaohui Yan
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摘要

环状 RNA(circRNA)作为新兴的生物标记物和调控因子,在医学诊断和治疗中的应用因其灵敏检测和精确调控所面临的挑战而受到阻碍。在此,我们开发了一种基于DNA四面体封闭催化DNA组装反应(DT-CDA)的高性能合作DNA纳米器件(HCDN),它既能成像,又能调控circRNAs。DT-CDA 的激活取决于目标 circRNA 的存在,目标 circRNA 与复制燃料探针一起催化了其他 DT-CDA 的依次打开。这种可忽略背景干扰的合作式指数信号放大使 HCDN 能够有效检测微量的 circRNA。以 circSATB2 为模型,HCDN 在细胞和体内模型中显示出 Cyclin D1 (CCND1) mRNA 和蛋白水平的大幅下调,从而抑制了肿瘤的生长。HCDN 的创新设计为增强临床诊断和生物分子操作的强大方法奠定了基础,从而推动了 DNA 纳米技术的能力和应用。
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High-Performance Cooperative DNA Nanodevice Enables Sensitive Circular RNA Imaging and Precise Tumor Growth Suppression
The utility of circular RNAs (circRNAs) as emerging biomarkers and regulatory factors in medical diagnostics and therapeutics is hampered by the challenges associated with their sensitive detection and precise modulation. Herein, a high-performance cooperative DNA nanodevice (HCDN) based on DNA tetrahedron-confined catalytic DNA assembly reaction (DT-CDA) that enables both imaging and regulation of circRNAs is developed. Activation of the DT-CDA is contingent upon the presence of the target circRNA, which, together with a replicative fuel probe, catalyzes the sequential opening of additional DT-CDAs. This cooperative exponential signal amplification with negligible background interference allows HCDN to effectively detect minute quantities of circRNAs. Employing circSATB2 as a model, the HCDN demonstrates substantial downregulation of Cyclin D1 (CCND1) mRNA and protein levels in cellular and in vivo models, thereby inhibiting tumor growth. The innovative design of HCDN sets the stage for a powerful methodology conducive to enhanced clinical diagnostics and biomolecule manipulation, thereby advancing the capabilities and applications of DNA nanotechnology.
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