Université Paris Diderot, Sorbonne Paris Cité, ITODYS, UMR 7086 CNRS, 15 rue J-A de Baïf, 75205 Paris Cedex 13, France; USTH, University of Science and Technology of Hanoi, 18 Hoang Quoc Viet, Hanoi, Vietnam; School of Chemical Engineering, Hanoi University of Science and Technology, 1st Dai Co Viet Road, Hanoi, Vietnam.
Université Paris Diderot, Sorbonne Paris Cité, ITODYS, UMR 7086 CNRS, 15 rue J-A de Baïf, 75205 Paris Cedex 13, France.
Biosens Bioelectron. 2014 Dec 15;62:25-30. doi: 10.1016/j.bios.2014.06.014. Epub 2014 Jun 14.
We design an electrochemical immunosensor for miRNA detection, based on screen-printed gold electrodes modified with reduced graphene oxide and carbon nanotubes. An original immunological approach is followed, using antibodies directed to DNA.RNA hybrids. An electrochemical ELISA-like amplification strategy was set up using a secondary antibody conjugated to horseradish peroxidase (HRP). Hydroquinone is oxidized into benzoquinone by the HRP/H2O2 catalytic system. In turn, benzoquinone is electroreduced into hydroquinone at the electrode. The catalytic reduction current is related to HRP amount immobilized on the surface, which itself is related to miRNA.DNA surface density on the electrode. This architecture, compared to classical optical detection, lowers the detection limit down to 10 fM. Two miRNAs were studied: miR-141 (a prostate biomarker) and miR-29b-1 (a lung cancer biomarker).
我们设计了一种基于还原氧化石墨烯和碳纳米管修饰的丝网印刷金电极的电化学免疫传感器,用于 miRNA 检测。采用针对 DNA.RNA 杂交体的抗体,遵循一种原始的免疫学方法。使用辣根过氧化物酶(HRP)偶联的二次抗体建立了电化学 ELISA 样放大策略。HRP/H2O2 催化体系将氢醌氧化成苯醌。苯醌反过来在电极上被电还原成氢醌。催化还原电流与固定在表面上的 HRP 量有关,而 HRP 量本身又与电极上的 miRNA.DNA 表面密度有关。与经典的光学检测相比,这种结构将检测限降低到 10 fM。研究了两种 miRNA:miR-141(前列腺生物标志物)和 miR-29b-1(肺癌生物标志物)。