School of the Environment and Safety Engineering , Jiangsu University , Zhenjiang 212013 , China.
Institute of Life Sciences , Jiangsu University , Zhenjiang 212013 , China.
Anal Chem. 2019 Jun 4;91(11):7353-7359. doi: 10.1021/acs.analchem.9b01133. Epub 2019 May 22.
MicroRNAs (miRNAs) play important roles as significant biomarkers in disease diagnostics. Here, an electrochemical biosensor was developed for the quick, sensitive, and specific detection of miRNAs from human-serum samples using three-dimensional (3D) DNA tetrahedron-structured probes (TSPs) and duplex-specific nuclease (DSN). The designed TSPs were composed of a recognition sequence that corresponded to a target miRNA and a G-quadruplex sequence that was combined with hemin to mimic the biocatalytic functions for HO reduction and l-cysteine oxidation. After hybridization with miRNA, the TSPs were immobilized on the Au electrode to shape the DNA-RNA double strands, which could be discriminated by DSN for hydrolysis of the DNA in the heteroduplexes to generate significant change in the reduction currents. Under optimal conditions, the biosensor showed a wide linear response ranging from 0.1 fM to 0.1 pM, with a low detection limit of 0.04 fM. Meanwhile, the method showed acceptable accuracy and precision for the determination of miRNAs in serum after a series of assessments.
微 RNA(miRNA)作为疾病诊断的重要生物标志物,发挥着重要作用。本研究构建了一种电化学生物传感器,通过三维(3D)DNA 四面体型探针(TSP)和双链特异性核酸酶(DSN),快速、灵敏、特异地检测人血清样本中的 miRNA。设计的 TSP 由与靶 miRNA 相对应的识别序列和与血红素结合的 G-四链体序列组成,模拟 HO 还原和 l-半胱氨酸氧化的生物催化功能。与 miRNA 杂交后,TSP 被固定在 Au 电极上形成 DNA-RNA 双链,DSN 可识别并水解异源双链体中的 DNA,从而产生还原电流的显著变化。在最优条件下,该生物传感器的线性响应范围为 0.1 fM 至 0.1 pM,检测限低至 0.04 fM。同时,经过一系列评估,该方法在血清中 miRNA 的测定中表现出良好的准确性和精密度。