...
首页> 外文期刊>International Journal of Nanomedicine >Sensitive detection of microRNAs based on the conversion of colorimetric assay into electrochemical analysis with duplex-specific nuclease-assisted signal amplification
【24h】

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

机译:基于比色测定转化为电化学分析的双链特异性核酸酶辅助信号扩增的灵敏检测microRNA

获取原文
   

获取外文期刊封面封底 >>

       

摘要

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.
机译:miRNA已成为检测多种癌症的新生物标记。通过采用双链特异性核酸酶进行信号放大,并使用金纳米颗粒(AuNPs)作为检测探针的载体,进行了miRNA的新型电化学检测。该方法基于将众所周知的比色测定法转换为具有增强灵敏度的电化学分析法。溶液中固定的DNA捕获探针和二茂铁(Fc)标记的DNA检测探针(表示为“ Fc-DNA-Fc”)通过静电相互作用在电极表面诱导了带正电的AuNP的组装。结果,大量的Fc-DNA-Fc分子附着在电极表面上,从而放大了电化学信号。当添加双链特异性核酸酶以回收miRNA启动的固定DNA探针消化过程时,在电极表面上不会发生Fc-DNA-Fc诱导的AuNP组装。这导致Fc的氧化电流显着下降。发现电流与miRNA的浓度成反比,范围为0-25 fM,检测极限为0.1 fM。此外,这项工作提出了一种将比色分析转换为敏感的电化学分析的新方法,因此对于新型化学/生物传感器的设计将是有价值的。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号