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基于功能 RNA 固定到 ITO/GNP 纳米图案上的 microRNA-155 的光谱电化学检测

Spectroelectrochemical detection of microRNA-155 based on functional RNA immobilization onto ITO/GNP nanopattern.

机构信息

Department of Chemical and Biomolecular Engineering, Sogang University, 35 Baekbeom-ro (Sinsu-dong), Mapo-gu, Seoul 121-742, Republic of Korea.

Department of Chemical Engineering, Kwangwoon University, 20 Kwangwoon-Ro, Nowon-Gu, Seoul 01897, Republic of Korea.

出版信息

J Biotechnol. 2018 May 20;274:40-46. doi: 10.1016/j.jbiotec.2018.03.014. Epub 2018 Mar 26.

DOI:10.1016/j.jbiotec.2018.03.014
PMID:29588181
Abstract

We fabricated a microRNA biosensor using the combination of surface enhanced Raman spectroscopy (SERS) and electrochemical (EC) techniques. For the first time, the weaknesses of each techniques for microRNA detection was compensated by the other ones to give rise to the specific and wide-range detection of miR-155. A single stranded 3' methylene blue (MB) and 5' thiol-modified RNA (MB-ssRNA-SH) was designed to detect the target miR-155 and immobilized onto the gold nanoparticle-modified ITO (ITO/GNP). Upon the invasion of target strand, the double-stranded RNA transformed rapidly to an upright structure resulting in a notable decrease in SERS and redox signals of the MB. For the first time, by combination of SERS and EC techniques in a single platform we extended the dynamic range of both techniques from 10 pM to 450 nM (SERS: 10 pM-5 nM and EC: 5 nM-450 nM). As well, the SERS technique improved the detection limit of the EC method from 100 pM to 100 fM, while the EC method covered single-mismatch detection which was the SERS deficiency. The fabricated single-step biosensor possessing a good capability of miRNA detection in human serum, could be employed throughout the broad ranges of biomedical and bioelectronics applications.

摘要

我们使用表面增强拉曼光谱 (SERS) 和电化学 (EC) 技术的组合制造了一种 microRNA 生物传感器。首次通过另一种技术来弥补每种技术在 microRNA 检测中的弱点,从而实现了对 miR-155 的特异性和宽范围检测。设计了一条单链 3' 亚甲基蓝 (MB) 和 5' 巯基修饰的 RNA (MB-ssRNA-SH),用于检测靶标 miR-155,并固定在金纳米粒子修饰的 ITO(ITO/GNP)上。在靶链入侵后,双链 RNA 迅速转化为直立结构,导致 MB 的 SERS 和氧化还原信号显著下降。首次在单个平台上将 SERS 和 EC 技术结合在一起,将两种技术的动态范围从 10 pM 扩展到 450 nM(SERS:10 pM-5 nM 和 EC:5 nM-450 nM)。此外,SERS 技术将 EC 方法的检测限从 100 pM 提高到 100 fM,而 EC 方法则涵盖了 SERS 技术的单碱基错配检测缺陷。该制造的单步生物传感器在人血清中具有良好的 microRNA 检测能力,可应用于广泛的生物医学和生物电子学应用中。

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