Biotechnology Division, Department of Molecular and Cell Biology, Faculty of Chemistry, University of Kashan, Kashan, Iran.
Department of Analytical Chemistry, Faculty of Chemistry, University of Kashan, Kashan, Iran.
Biosens Bioelectron. 2016 Mar 15;77:202-7. doi: 10.1016/j.bios.2015.09.025. Epub 2015 Sep 16.
Small noncoding microRNAs (miRNAs) have emerged as ideal noninvasive biomarkers for early-phase cancer detection. In this report, a label-free and simple electrochemical miRNA biosensor is developed based on employing methylene blue (MB) as a redox indicator. The successfully immobilization of the single strand DNA (ss-DNA) probe and hybridization with the target miRNA sequence were confirmed by electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV) methods. Differential pulse voltammetry (DPV) technique was used to record the oxidation peak current of MB under optimal condition and an increase in the peak current was observed after hybridization. By employing this strategy, miRNA can detect in a range from 0.1 to 500.0 pM with a relatively low detection limit of 84.3 fM. The electrochemical response of MB on ss-DNA and duplex of miRNA/DNA was characterized by CV and chronocoulometry method. The linear relation between the redox peak currents (Ip) and scan rate (ν) indicates that the electron transfer (ET) between MB and the electrode surface was mediated by the miRNA/DNA π-stacked duplex. The value of surface coverage (Γ) was calculated that indicated increase amount of MB on the surface of modified electrode after hybridization event and revealed the adsorption of MB at modified electrode is monolayer. Also, the electron transfer rate constants (ks) of MB were estimated. The results of kinetic analysis were confirmed by chronocoulometry method. The discrimination ability of miRNA biosensor even against a noncomplementary target was also studied. Consequently, this strategy will be valuable for sensitive, selective and label-free detection of miRNA.
小分子非编码 microRNAs(miRNAs)已成为早期癌症检测的理想非侵入性生物标志物。在本报告中,开发了一种基于使用亚甲基蓝(MB)作为氧化还原指示剂的无标记和简单的电化学 miRNA 生物传感器。通过电化学阻抗谱(EIS)和循环伏安法(CV)方法证实了单链 DNA(ss-DNA)探针的成功固定和与靶 miRNA 序列的杂交。差分脉冲伏安法(DPV)技术用于在最佳条件下记录 MB 的氧化峰电流,并在杂交后观察到峰电流增加。通过采用这种策略,可以在 0.1 至 500.0 pM 的范围内检测 miRNA,检测限相对较低,为 84.3 fM。通过 CV 和计时库仑法对 MB 在 ss-DNA 和 miRNA/DNA 双链体上的电化学响应进行了表征。MB 的氧化峰电流(Ip)与扫描速率(ν)之间的线性关系表明,MB 与电极表面之间的电子转移(ET)是由 miRNA/DNA π 堆积双链介导的。计算了表面覆盖率(Γ)的值,表明杂交事件后修饰电极表面上 MB 的增加量,并表明 MB 在修饰电极上的吸附是单层的。还估计了 MB 的电子转移速率常数(ks)。通过计时库仑法对动力学分析结果进行了验证。还研究了 miRNA 生物传感器甚至对非互补靶标的区分能力。因此,该策略将有助于 miRNA 的灵敏、选择性和无标记检测。