All-In-One Entropy-Driven DNA Nanomachine for Tumor Cell-Selective Fluorescence/SERS Dual-Mode Imaging of MicroRNA

被引:1
|
作者
Yue, Shuzhen [1 ,2 ]
Xu, Xuan [1 ]
Jiang, Li-Ping [1 ]
Yao, Huiqin [3 ]
Zhu, Jun-Jie [1 ]
机构
[1] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Analyt Chem Life Sci, Nanjing 210023, Peoples R China
[2] Linyi Univ, Coll Med, Shandong Prov Key Lab Detect Technol Tumor Markers, Linyi 276005, Peoples R China
[3] Ningxia Med Univ, Coll Basic Med, Dept Med Chem, Yinchuan 750004, Peoples R China
基金
中国国家自然科学基金;
关键词
D O I
10.1021/acs.analchem.4c05256
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An entropy-driven catalysis (EDC) strategy is appealing for amplified bioimaging of microRNAs in living cells; yet, complex operation procedures, lacking of cell selectivity, and insufficient accuracy hamper its further applications. Here, we introduce an ingenious all-in-one entropy-driven DNA nanomachine (termed as AIO-EDN), which can be triggered by endogenous apurinic/apyrimidinic endonuclease 1 (APE1) to achieve tumor cell-selective dual-mode imaging of microRNA. Compared with the traditional EDC strategy, the integrated design of AIO-EDN achieves autocatalytic signal amplification without extra fuel strands. Moreover, the AIO-EDN leverages an endogenous APE1 overexpressed in cancer cells to activate the EDC reaction, which, however, exerts no target sensing activity in normal cells. Combining fluorescence- and surface-enhanced Raman scattering (FL/SERS) dual-mode imaging techniques, this DNA nanomachine exhibits significantly improved accuracy and tumor cell selectivity for microRNA imaging in living cells. This study provides a new paradigm to develop an integrated EDC-based platform and shows great potential in in-depth cancer diagnosis with high precision.
引用
收藏
页码:1739 / 1747
页数:9
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