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基于氨基功能化石墨烯量子点和 ss-DNA 与 ds-DNA 作为基因探针的 microRNA-25 的伏安测定法。

A voltammetric assay for microRNA-25 based on the use of amino-functionalized graphene quantum dots and ss- and ds-DNAs as gene probes.

机构信息

Department of Chemistry, Faculty of Science, Yazd University, Yazd, 89195-741, Iran.

出版信息

Mikrochim Acta. 2018 Oct 9;185(11):503. doi: 10.1007/s00604-018-3037-6.

Abstract

The authors describe a DNA based voltammetric assay for the cancer biomarker microRNA-25. A glassy carbon electrode (GCE) was modified with amino-functionalized graphene quantum dots and used as an amplifier of electrochemical signals. p-Biphenol is introduced as a new electroactive probe with a fairly low working potential of 0.3 V (vs. Ag/AgCl). The stages of fabricating the electrode were characterized by cyclic voltammetry and electrochemical impedance spectroscopy. ss-Probe DNA was immobilized on the modified GCE and then exposed to a sample containing microRNA-25. The results indicated that the electrode can distinguish complementary microRNA-25 from a single-base mismatch. The increase in the electrochemical response of PBP and the positive shift in the potential peak indicate that PBP is intercalated between two strands. Under optimized experimental conditions, the current of the electrode increases linearly with the logarithm of the microRNA-25 concentration in the range from 0.3 nM to 1.0 μM, and the detection limit is 95.0 pM. The assay was successfully employed to the determination of microRNA-25 in spiked human plasma. Graphical abstract A novel electrochemical nanogenosensor is introduced for simple and sensitive determination of microRNA-25, as a biomarker, based on amino-functionalized graphene quantum dots (as a surface modifier) and p-biphenol (as an electroactive label).

摘要

作者描述了一种基于 DNA 的用于癌症生物标志物 microRNA-25 的伏安测定法。玻碳电极(GCE)经氨基功能化石墨烯量子点修饰,用作电化学信号的放大器。对苯二酚被引入作为一种新的电化学活性探针,其工作电位相当低,为 0.3 V(相对于 Ag/AgCl)。制造电极的各个阶段都通过循环伏安法和电化学阻抗谱进行了表征。ss-Probe DNA 固定在修饰的 GCE 上,然后暴露于含有 microRNA-25 的样品中。结果表明,该电极可以区分互补的 microRNA-25 与单碱基错配。PBP 的电化学响应增加和电位峰的正向移动表明 PBP 插入到两条链之间。在优化的实验条件下,电极的电流与 microRNA-25 浓度的对数在 0.3 nM 至 1.0 μM 的范围内呈线性增加,检测限为 95.0 pM。该测定法成功地用于测定人血浆中 microRNA-25 的含量。

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