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靶向触发的纳腔天线组装以增强单个分子的荧光及其在 microRNA 检测中的应用。

Target-Triggered Assembly of Nanogap Antennas to Enhance the Fluorescence of Single Molecules and Their Application in MicroRNA Detection.

机构信息

State Key Laboratory of Theoretical and Computational Photochemistry, Ministry of Education, College of Chemistry, Beijing Normal University, Beijing, 100875, China.

出版信息

Small. 2020 May;16(19):e2000460. doi: 10.1002/smll.202000460. Epub 2020 Apr 20.

Abstract

Nanogap antennas are plasmonic nanostructures with a strong electromagnetic field generated at the gap region of two neighboring particles owing to the coupling of the collective surface plasmon resonance. They have great potential for improving the optical properties of fluorophores. Herein, nanogap antennas are constructed using an aqueous solution-based method to overcome the defects of weak fluorescence and photobleaching associated with traditional organic dyes, and a highly sensitive nanogap antenna-based sensing strategy is presented for the detection of low-abundance nucleic acid biomarkers via a target-triggered strand displacement amplification (SDA) reaction between two DNA hairpins that are tagged to the tips of gold nanorods (Au NRs). In the presence of targets, end-to-end Au NR dimers gradually form, and the fluorophores quenched by the Au NRs exhibit a dramatic fluorescence enhancement due to the plasmon-enhanced fluorescence effect of nanogap antennas. Meanwhile, the SDA reaction results in secondary amplification of fluorescence signals. Combined with single-molecule counting, this method applied in miRNA-21 detection can achieve a low detection limit of 97.2 × 10 m. Moreover, accurate discrimination between different cells through miRNA-21 imaging demonstrates the potential of this method in monitoring the expression level of low-abundance nucleic acid biomarkers.

摘要

纳米间隙天线是一种等离子体纳米结构,由于两个相邻粒子的集体表面等离激元共振的耦合,在间隙区域会产生强电磁场。它们在改善荧光团的光学性质方面具有很大的潜力。在此,通过基于水溶液的方法构建了纳米间隙天线,以克服传统有机染料的荧光弱和光漂白缺陷,并提出了一种基于纳米间隙天线的高灵敏度传感策略,用于通过标记在金纳米棒(Au NRs)尖端的两个 DNA 发夹之间的靶触发链置换扩增(SDA)反应检测低丰度核酸生物标志物。在存在靶标时,Au NR 二聚体逐渐形成,由于纳米间隙天线的等离子体增强荧光效应,被 Au NR 猝灭的荧光团表现出明显的荧光增强。同时,SDA 反应导致荧光信号的二次放大。结合单分子计数,该方法应用于 miRNA-21 的检测可达到 97.2×10 m 的低检测限。此外,通过 miRNA-21 成像对不同细胞进行准确区分,证明了该方法在监测低丰度核酸生物标志物表达水平方面的潜力。

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