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

IF 6.7 1区 化学 Q1 CHEMISTRY, ANALYTICAL Analytical Chemistry Pub Date : 2025-01-13 DOI:10.1021/acs.analchem.4c05256
Shuzhen Yue, Xuan Xu, Li-Ping Jiang, Huiqin Yao, Jun-Jie Zhu
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Abstract

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.

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用于肿瘤细胞选择性 MicroRNA 荧光/SERS 双模式成像的一体化熵驱动 DNA 纳米机器
熵驱动催化(EDC)策略对活细胞中微小rna的放大生物成像具有吸引力;然而,复杂的操作程序、缺乏细胞选择性和精度不足阻碍了它的进一步应用。在这里,我们介绍了一种巧妙的一体化熵驱动DNA纳米机器(称为AIO-EDN),它可以由内源性无尿嘧啶/无嘧啶内切酶1 (APE1)触发,以实现肿瘤细胞选择性microRNA的双模式成像。与传统的EDC策略相比,AIO-EDN的一体化设计实现了自催化信号放大,无需额外的燃料链。此外,AIO-EDN利用癌细胞中过表达的内源性APE1来激活EDC反应,而该反应在正常细胞中没有靶标感应活性。结合荧光和表面增强拉曼散射(FL/SERS)双模成像技术,该DNA纳米机器在活细胞中对microRNA成像的准确性和肿瘤细胞选择性显着提高。该研究为开发基于edc的集成平台提供了新的范例,在高精度的癌症深度诊断方面具有很大的潜力。
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来源期刊
Analytical Chemistry
Analytical Chemistry 化学-分析化学
CiteScore
12.10
自引率
12.20%
发文量
1949
审稿时长
1.4 months
期刊介绍: Analytical Chemistry, a peer-reviewed research journal, focuses on disseminating new and original knowledge across all branches of analytical chemistry. Fundamental articles may explore general principles of chemical measurement science and need not directly address existing or potential analytical methodology. They can be entirely theoretical or report experimental results. Contributions may cover various phases of analytical operations, including sampling, bioanalysis, electrochemistry, mass spectrometry, microscale and nanoscale systems, environmental analysis, separations, spectroscopy, chemical reactions and selectivity, instrumentation, imaging, surface analysis, and data processing. Papers discussing known analytical methods should present a significant, original application of the method, a notable improvement, or results on an important analyte.
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