Electrochemiluminescence biosensor for miRNA-21 based on toehold-mediated strand displacement amplification with Ru(phen)32+ loaded DNA nanoclews as signal tags

电化学发光 DNA 多重位移放大 滚动圆复制 检出限 生物传感器 复式(建筑) 化学 信号(编程语言) 组合化学 生物物理学 纳米技术 材料科学 聚合酶链反应 生物 聚合酶 计算机科学 生物化学 色谱法 基因 DNA提取 程序设计语言
作者
Ying Zhang,Guoyan Xu,Guili Lian,Fang Luo,Qunfang Xie,Zhenyu Lin,Guonan Chen
出处
期刊:Biosensors and Bioelectronics [Elsevier BV]
卷期号:147: 111789-111789 被引量:72
标识
DOI:10.1016/j.bios.2019.111789
摘要

A novel electrochemiluminescence (ECL) biosensor was developed for high sensitive and selective detection of miRNA-21 based on the efficient and specific toehold-mediated strand displacement (TMSD) amplification with Ru(phen)32+ loaded DNA nanoclews (NCs–Ru(phen)32+) as signal tags. The stable DNA nanoclews, synthesized by a simple rolling circle amplification reaction, were employed to load with Ru(phen)32+ efficiently as ECL signal tags to amplify the signals. As for TMSD, the substrate strand (Sub) was initially hybridized with P1 and P2 to form DNA duplex structures with a toehold 1. miRNA-21 could hybridize with the toehold 1 and trigger the TMSD amplification with the help of assist strand, releasing lots of P1 stands from DNA duplex structures. The TMSD technique realized the converting and amplification of the single miRNA-21 input to lots of output DNA (namely P1) with good selectivity, simultaneously. Output P1 were designed to expand the stem-locked region of HP, which were immobilized on the Au electrodes firstly. Subsequently, the opened HP could hybridize with the Ru(phen)32+, capturing the ECL signal tags closed to the sensing surface. The ECL intensity of the system had a linear relationship with the logarithm of the miRNA-21 concentration in the range of 1.0 fM to 100 pM with a limit of detection of 0.65 fM. The strategy was further applied to detect miRNA-21 in complex samples, and the result was consistent with the qRT-PCR.
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