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基于单液流通道的电化学 DNA 芯片的多重实时环介导等温扩增。

Multiplex Real-Time Loop-Mediated Isothermal Amplification Using an Electrochemical DNA Chip Consisting of a Single Liquid-Flow Channel.

机构信息

Corporate Research & Development Center, Research & Development Division , Toshiba Corporation , 1 Komukai-Toshiba-cho , Saiwai-ku, Kawasaki 212-8582 , Japan.

出版信息

Anal Chem. 2019 Mar 5;91(5):3227-3232. doi: 10.1021/acs.analchem.8b05284. Epub 2019 Feb 19.

Abstract

We developed a multiplex system capable of simultaneously quantifying different target sequences by applying an electrochemical DNA chip that consists of single liquid-flow channel with primers designed for loop-mediated isothermal amplification (LAMP). We applied this system for detecting mature microRNAs (miRNAs). miRNAs extracted from serum were enzymatically lengthened to about 100 base pairs by reverse-transcription and elongation reactions. The LAMP primers for amplifying the lengthened miRNAs were adsorbed and immobilized on the surface of the liquid-flow channel at five different positions. A LAMP solution containing the lengthened miRNAs, Tin DNA polymerase, and ruthenium hexaamine (RuHex) as a redox compound was injected into the DNA chip. The electrochemical reaction of RuHex in the LAMP solution was then measured continuously via linear-sweep voltammetry at 65 °C. The LAMP reaction of the positive control revealed that the cathodic peak current of RuHex increased. Additionally, the initial number of miRNA copies was correlated with the time when the cathodic current began to increase. Five miRNAs were simultaneously detected at 10-10 copies per 50 μL within 2 h. We expect these results will be useful for developing a simple and stable electrochemical-based method for the real-time monitoring of miRNAs, while also facilitating the implementation of electrochemical DNA chips for molecular analyses.

摘要

我们开发了一种多重系统,能够通过应用电化学 DNA 芯片同时定量不同的靶序列,该芯片由具有用于环介导等温扩增 (LAMP) 的引物的单个液流通道组成。我们将该系统应用于检测成熟 microRNAs (miRNAs)。从血清中提取的 miRNAs 通过反转录和延伸反应被酶促延长至约 100 个碱基对。用于扩增延长的 miRNAs 的 LAMP 引物被吸附并固定在液流通道的五个不同位置上。含有延长的 miRNAs、Tin DNA 聚合酶和钌六胺 (RuHex) 的 LAMP 溶液被注入 DNA 芯片。然后通过线性扫描伏安法在 65°C 下连续测量 LAMP 溶液中 RuHex 的电化学反应。阳性对照的 LAMP 反应表明 RuHex 的阴极峰电流增加。此外,miRNA 拷贝的初始数量与阴极电流开始增加的时间相关。在 2 小时内,5 种 miRNAs 可以在 50 μL 内以 10-10 拷贝的浓度同时检测到。我们希望这些结果将有助于开发一种简单稳定的基于电化学的 miRNA 实时监测方法,同时也有助于电化学 DNA 芯片在分子分析中的应用。

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