Chen Yingying, Gong Xue, Gao Yuhui, Shang Yu, Shang Jinhua, Yu Shanshan, Li Ruomeng, He Shizhen, Liu Xiaoqing, Wang Fuan
College of Chemistry and Molecular Sciences, Wuhan University Wuhan 430072 P. R. China.
Research Institute of Shenzhen, Wuhan University Shenzhen 518057 P. R. China
Chem Sci. 2021 Nov 8;12(47):15710-15718. doi: 10.1039/d1sc05214d. eCollection 2021 Dec 8.
Catalytic DNA circuits represent a versatile toolbox for tracking intracellular biomarkers yet are constrained with low anti-interference capacity originating from their severe off-site activation. Herein, by introducing an unprecedented endogenous DNA repairing enzyme-powered pre-selection strategy, we develop a sequential and specific on-site activated catalytic DNA circuit for achieving the cancer cell-selective imaging of microRNA with high anti-interference capacity. Initially, the circuitry reactant is firmly caged by an elongated stabilizing duplex segment with a recognition/cleavage site of a cell-specific DNA repairing enzyme, which can prevent undesired signal leakage prior to its exposure to target cells. Then, the intrinsic DNA repairing enzyme of target cells can liberate the DNA probe for efficient intracellular microRNA imaging the multiply guaranteed molecular recognition/activation procedures. This bioorthogonal regulated DNA circuit presents a modular and programmable amplification strategy for highly reliable assays of intracellular biomarkers, and provides a pivotal molecular toolbox for living systems.
催化性DNA电路是用于追踪细胞内生物标志物的多功能工具盒,但由于其严重的非位点激活导致抗干扰能力较低而受到限制。在此,通过引入一种前所未有的内源性DNA修复酶驱动的预筛选策略,我们开发了一种顺序且特异性的原位激活催化DNA电路,用于实现具有高抗干扰能力的癌细胞选择性微小RNA成像。最初,电路反应物被一个带有细胞特异性DNA修复酶识别/切割位点的延长稳定双链片段牢固地封闭,这可以防止在其暴露于靶细胞之前出现不必要的信号泄漏。然后,靶细胞的内源性DNA修复酶可以释放DNA探针,用于通过多重保证的分子识别/激活程序进行高效的细胞内微小RNA成像。这种生物正交调节的DNA电路为细胞内生物标志物的高度可靠检测提供了一种模块化和可编程的放大策略,并为生命系统提供了一个关键的分子工具盒。