化学
小RNA
内生
刺激
DNA
酶
生物物理学
组合化学
生物化学
神经科学
基因
生物
作者
Yuqian Jiang,Chenxia Xie,Yingying Chen,Hui Wang,Jinhua Shang,Xiaoqing Liu,Fuan Wang
标识
DOI:10.1021/acs.analchem.5c03309
摘要
Localized DNA circuits have emerged as a powerful platform for real-time visualization of disease-associated biomolecules in living cells, enabling deeper insights into complex biological processes. However, their extensive applications have been limited by a low probe utilization efficiency and nonspecific background signals. Here, we present a cell-specifically triggered localized catalytic assembly (TCA) circuit designed for high-contrast, reliable imaging of microRNAs (miRNAs). The TCA system features a modular architecture in which an aptamer-mediated targeting module and an endogenously activated sensing module are integrated into a single multifunctional probe. This design enables sequential targeted delivery, target-induced probe activation, and localized sensing of the intracellular miRNA. The integrated strategy significantly improves the probe utilization efficiency and reaction kinetics while suppressing off-target background signals. As a result, it enables high-contrast, accurate imaging of miRNAs and precise discrimination between cancerous and normal cells. Furthermore, we demonstrate its utility in reliably assessing chemotherapy-induced drug resistance in cancer cells. Thus, the TCA circuit provides a robust platform for intracellular biomolecular monitoring and probing of drug-resistance-related molecular mechanisms, highlighting its potential applications in molecular diagnostics and precision medicine.
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