Center for Molecular Recognition and Biosensing, School of Life Sciences, Shanghai University, 200444, PR China.
Center for Molecular Recognition and Biosensing, School of Life Sciences, Shanghai University, 200444, PR China.
Biosens Bioelectron. 2019 Apr 1;130:132-138. doi: 10.1016/j.bios.2019.01.024. Epub 2019 Jan 18.
In this work, DNA-templated silver nanoclusters (DNA-AgNCs) with unique fluorescent and electrochemical properties are prepared as dual signal probes for both qualitative imaging and quantitative detection of cancer cells in an integrated system. ITO electrode that has good light transmittance and electric conductivity is employed as a substrate for dual analysis of cancer cells. ITO electrode is firstly modified by AS1141 aptamer, which could selectively bind to nucleolin overexpressed on the surface of a model breast cancer cell, MCF-7 cell line. The composite of mucin 1 antibody (anti-MUC1) and DNA-AgNCs then binds to MUC1 on the surface of captured MCF-7 cell, forming a sandwich-like structure. Therefore, our method allows noninvasive fluorescence imaging and amplified electrochemical detection using a single labeling platform, providing a biocompatible and highly specific method for adequate analysis of cancer cells. Experimental results demonstrate that strong red fluorescence of DNA-AgNCs clearly displays the loading of cancer cells on ITO electrode after dual recognition, and amplified electrochemical signals of DNA-AgNCs enable improved sensitivity toward quantitative analysis with a detection limit of 3 cells.
在这项工作中,制备了具有独特荧光和电化学性质的 DNA 模板银纳米簇(DNA-AgNCs),作为双信号探针,用于集成系统中癌细胞的定性成像和定量检测。具有良好透光率和导电性的 ITO 电极被用作癌细胞双重分析的基底。ITO 电极首先通过 AS1141 适体进行修饰,该适体能特异性地与模型乳腺癌细胞 MCF-7 表面过度表达的核仁素结合。然后,粘蛋白 1 抗体(抗-MUC1)和 DNA-AgNCs 的复合物与捕获的 MCF-7 细胞表面的 MUC1 结合,形成三明治样结构。因此,我们的方法允许使用单个标记平台进行非侵入性荧光成像和放大电化学检测,为充分分析癌细胞提供了一种生物相容性和高度特异性的方法。实验结果表明,DNA-AgNCs 的强红色荧光在双重识别后清晰地显示了癌细胞在 ITO 电极上的加载,并且 DNA-AgNCs 的放大电化学信号能够提高定量分析的灵敏度,检测限为 3 个细胞。