Electronic Detection of Micro RNA Mir2O6 with Molecularly-Differentiated Nanoelectrodes

Jianchun Dong, A. Asawachaicharn, S. Tapscott, B. Parviz
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引用次数: 1

Abstract

Micro RNAs (miRNAs) play important roles in gene regulation at the translational level. However up to this date, there still lacks a fast and efficient method for its detection and quantification. In this paper, we present the construction and characterization of a nanoelectrode sensor array capable of detecting the presence of micro RNA (miRNA) molecules and directly converting their hybridization with an immobilized probe into an electrical signal. Each sensing unit in the array consists of three nano-scale electrodes: counter, control, and working. Electrochemical desorption is used to program the attachment of DNA oligonucleotides complementary to the target miRNA on the working electrode and a nonfouling poly(ethyleneglycol) (PEG) terminated molecular monolayer on the control and counter electrodes. The current flowing between the electrodes is monitored and the capture and hybridization of the target miRNA is verified via measurement of the differential conductance signals.
分子分化纳米电极对微RNA Mir2O6的电子检测
微rna (miRNAs)在翻译水平的基因调控中起着重要作用。但迄今为止,仍缺乏一种快速有效的检测和定量方法。在本文中,我们介绍了一种纳米电极传感器阵列的构建和表征,该阵列能够检测微RNA (miRNA)分子的存在,并直接将其与固定探针的杂交转化为电信号。阵列中的每个传感单元由三个纳米级电极组成:计数器、控制和工作电极。电化学解吸用于编程与目标miRNA互补的DNA寡核苷酸在工作电极上的附着,以及在对照电极和反电极上的无污染聚乙二醇(PEG)端接分子单层。监测电极之间的电流流动,并通过测量差分电导信号验证目标miRNA的捕获和杂交。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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