Recent Progresses in Electrochemical DNA Biosensors for MicroRNA Detection.

IF 3.7 Q2 GENETICS & HEREDITY
Phenomics (Cham, Switzerland) Pub Date : 2022-01-21 eCollection Date: 2022-02-01 DOI:10.1007/s43657-021-00032-z
Lulu Zhang, Wenqiong Su, Shuopeng Liu, Chengjie Huang, Behafarid Ghalandari, Adeleh Divsalar, Xianting Ding
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Abstract

MicroRNAs (miRNAs), as the small, non-coding, evolutionary conserved, and post-transcriptional gene regulators of the genome, have been highly associated with various diseases such as cancers, viral infections, and cardiovascular diseases. Several techniques have been established to detect miRNAs, including northern blotting, real-time polymerase chain reaction (RT-PCR), and fluorescent microarray platform. However, it remains a significant challenge to develop sensitive, accurate, rapid, and cost-effective methods to detect miRNAs due to their short size, high similarity, and low abundance. The electrochemical biosensors exhibit tremendous potential in miRNA detection because they satisfy feature integration, portability, mass production, short response time, and minimal sample consumption. This article reviewed the working principles and signal amplification strategies of electrochemical DNA biosensors summarized the recent improvements. With the development of DNA nanotechnology, nanomaterials and biotechnology, electrochemical DNA biosensors of high sensitivity and specificity for microRNA detection will shortly be commercially accessible.

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Abstract Image

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用于 MicroRNA 检测的电化学 DNA 生物传感器的最新进展。
微小核糖核酸(miRNA)是一种小型、非编码、进化保守、转录后的基因调控因子,与癌症、病毒感染和心血管疾病等多种疾病高度相关。目前已建立了多种检测 miRNA 的技术,包括 Northern 印迹、实时聚合酶链反应(RT-PCR)和荧光芯片平台。然而,由于 miRNAs 体积小、相似性高、丰度低,要开发灵敏、准确、快速和经济有效的方法来检测它们仍是一项重大挑战。电化学生物传感器在 miRNA 检测方面展现出巨大的潜力,因为它具有集成、便携、可大规模生产、响应时间短和样品消耗少等特点。本文综述了电化学 DNA 生物传感器的工作原理和信号放大策略,总结了近年来的改进。随着 DNA 纳米技术、纳米材料和生物技术的发展,用于 microRNA 检测的高灵敏度和高特异性的电化学 DNA 生物传感器将很快实现商业化。
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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