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基于双链特异性核酸酶辅助信号放大将比色法转化为电化学分析的微小RNA的灵敏检测

Sensitive detection of microRNAs based on the conversion of colorimetric assay into electrochemical analysis with duplex-specific nuclease-assisted signal amplification.

作者信息

Xia Ning, Liu Ke, Zhou Yingying, Li Yuanyuan, Yi Xinyao

机构信息

Key Laboratory of New Optoelectronic Functional Materials, College of Chemistry and Chemical Engineering, Anyang Normal University, Anyang.

College of Chemistry and Chemical Engineering, Central South University, Changsha, China.

出版信息

Int J Nanomedicine. 2017 Jul 13;12:5013-5022. doi: 10.2147/IJN.S138656. eCollection 2017.

Abstract

miRNAs have emerged as new biomarkers for the detection of a wide variety of cancers. By employing duplex-specific nuclease for signal amplification and gold nanoparticles (AuNPs) as the carriers of detection probes, a novel electrochemical assay of miRNAs was performed. The method is based on conversion of the well-known colorimetric assay into electrochemical analysis with enhanced sensitivity. DNA capture probes immobilized on the electrode surface and ferrocene (Fc)-labeled DNA detection probes (denoted "Fc-DNA-Fc") presented in the solution induced the assembly of positively charged AuNPs on the electrode surface through the electrostatic interaction. As a result, a large number of Fc-DNA-Fc molecules were attached on the electrode surface, thus amplifying the electrochemical signal. When duplex-specific nuclease was added to recycle the process of miRNA-initiated digestion of the immobilized DNA probes, Fc-DNA-Fc-induced assembly of AuNPs on the electrode surface could not occur. This resulted in a significant fall in the oxidation current of Fc. The current was found to be inversely proportional to the concentration of miRNAs in the range of 0-25 fM, and a detection limit of 0.1 fM was achieved. Moreover, this work presents a new method for converting colorimetric assays into sensitive electrochemical analyses, and thus would be valuable for design of novel chemical/biosensors.

摘要

微小RNA(miRNAs)已成为检测多种癌症的新型生物标志物。通过使用双链特异性核酸酶进行信号放大,并以金纳米颗粒(AuNPs)作为检测探针的载体,开展了一种新型的miRNAs电化学检测方法。该方法基于将著名的比色法转化为具有更高灵敏度的电化学分析方法。固定在电极表面的DNA捕获探针与溶液中呈现的二茂铁(Fc)标记的DNA检测探针(表示为“Fc-DNA-Fc”)通过静电相互作用诱导带正电荷的AuNPs在电极表面组装。结果,大量的Fc-DNA-Fc分子附着在电极表面,从而放大了电化学信号。当加入双链特异性核酸酶以循环miRNA引发的固定化DNA探针消化过程时,Fc-DNA-Fc诱导的AuNPs在电极表面的组装就不会发生。这导致Fc的氧化电流显著下降。发现电流在0 - 25 fM范围内与miRNAs的浓度成反比,检测限达到0.1 fM。此外,这项工作提出了一种将比色法转化为灵敏电化学分析的新方法,因此对于新型化学/生物传感器的设计具有重要价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1b5/5516875/04342953d92d/ijn-12-5013Fig1.jpg

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