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基于 DNA 链置换的适体传感器的表面增强拉曼散射研究——利用 Au-Ag 双金属纳米枝晶基底

Toehold-mediated DNA displacement-based surface-enhanced Raman scattering DNA sensor utilizing an Au-Ag bimetallic nanodendrite substrate.

机构信息

Department of Chemistry, College of Natural Sciences, Hanyang University, Seoul 133-791, Republic of Korea.

Department of Chemistry, Research Institute for Basic Sciences, Kyung Hee University, Seoul 130-701, Republic of Korea.

出版信息

Anal Chim Acta. 2015 Jul 23;885:132-9. doi: 10.1016/j.aca.2015.04.037. Epub 2015 Apr 21.

Abstract

A simple and sensitive surface enhanced Raman scattering (SERS)-based DNA sensor that utilizes the toehold-mediated DNA displacement reaction as a target-capturing scheme has been demonstrated. For a SERS substrate, Au-Ag bimetallic nanodendrites were electrochemically synthesized and used as a sensor platform. The incorporation of both Ag and Au was employed to simultaneously secure high sensitivity and stability of the substrate. An optimal composition of Ag and Au that satisfied these needs was determined. A double-strand composed of 'a probe DNA (pDNA)' complementary to 'a target DNA (tDNA)' and 'an indicator DNA tagged with a Raman reporter (iDNA)' was conjugated on the substrate. The conjugation made the reporter molecule close to the surface and induced generation of the Raman signal. The tDNA released the pre-hybridized iDNA from the pDNA via toehold-mediated displacement, and the displacement of the iDNA resulted in the decrease of Raman intensity. The variation of percent intensity change was sensitive and linear in the concentration range from 200fM to 20nM, and the achieved limit of detection (LOD) was 96.3fM, superior to those reported in previous studies that adopted different signal taggings based on such as fluorescence and electrochemistry.

摘要

一种简单灵敏的基于表面增强拉曼散射(SERS)的 DNA 传感器,利用引发链介导的 DNA 置换反应作为目标捕获方案。对于 SERS 基底,采用电化学合成了 Au-Ag 双金属纳米枝晶,并将其用作传感器平台。同时引入 Ag 和 Au 以确保基底具有高灵敏度和稳定性。确定了满足这些需求的最佳 Ag 和 Au 组成。双链由与“靶 DNA(tDNA)”互补的“探针 DNA(pDNA)”和带有拉曼报告分子的“指示剂 DNA(iDNA)”组成,连接在基底上。这种连接使报告分子靠近表面,并诱导拉曼信号的产生。tDNA 通过引发链介导的置换从 pDNA 上释放出预杂交的 iDNA,iDNA 的置换导致拉曼强度的降低。强度变化百分比的变化在 200fM 至 20nM 的浓度范围内是敏感和线性的,并且实现的检测限(LOD)为 96.3fM,优于先前研究中采用基于荧光和电化学等不同信号标记的研究报告的 LOD。

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