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基于正电荷金纳米粒子猝灭银纳米团簇的荧光实现 miRNA 无标记检测的平台。

Label-Free Platform for MicroRNA Detection Based on the Fluorescence Quenching of Positively Charged Gold Nanoparticles to Silver Nanoclusters.

机构信息

School of Life Science, and ‡School of Chemistry and Materials Science, Jiangsu Normal University , Xuzhou 221116, China.

出版信息

Anal Chem. 2018 Jan 16;90(2):1098-1103. doi: 10.1021/acs.analchem.7b01991. Epub 2017 Dec 21.

Abstract

A novel strategy was developed for microRNA-155 (miRNA-155) detection based on the fluorescence quenching of positively charged gold nanoparticles [(+)AuNPs] to Ag nanoclusters (AgNCs). In the designed system, DNA-stabilized Ag nanoclusters (DNA/AgNCs) were introduced as fluorescent probes, and DNA-RNA heteroduplexes were formed upon the addition of target miRNA-155. Meanwhile, the (+)AuNPs could be electrostatically adsorbed on the negatively charged single-stranded DNA (ssDNA) or DNA-RNA heteroduplexes to quench the fluorescence signal. In the presence of duplex-specific nuclease (DSN), DNA-RNA heteroduplexes became a substrate for the enzymatic hydrolysis of the DNA strand to yield a fluorescence signal due to the diffusion of AgNCs away from (+)AuNPs. Under the optimal conditions, (+)AuNPs displayed very high quenching efficiency to AgNCs, which paved the way for ultrasensitive detection with a low detection limit of 33.4 fM. In particular, the present strategy demonstrated excellent specificity and selectivity toward the detection of target miRNA against control miRNAs, including mutated miRNA-155, miRNA-21, miRNA-141, let-7a, and miRNA-182. Moreover, the practical application value of the system was confirmed by the evaluation of the expression levels of miRNA-155 in clinical serum samples with satisfactory results, suggesting that the proposed sensing platform is promising for applications in disease diagnosis as well as the fundamental research of biochemistry.

摘要

基于正电荷金纳米粒子 [(+)AuNPs] 对银纳米簇 (AgNCs) 的荧光猝灭作用,开发了一种用于 microRNA-155 (miRNA-155) 检测的新策略。在设计的系统中,引入了 DNA 稳定的银纳米簇 (DNA/AgNCs) 作为荧光探针,并且在添加靶 miRNA-155 后形成 DNA-RNA 杂合体。同时,(+)AuNPs 可以通过静电吸附在带负电荷的单链 DNA (ssDNA) 或 DNA-RNA 杂合体上,从而猝灭荧光信号。在双链特异性核酸酶 (DSN) 的存在下,DNA-RNA 杂合体成为 DNA 链酶促水解的底物,由于 AgNCs 从 (+)AuNPs 扩散,从而产生荧光信号。在最佳条件下,(+)AuNPs 对 AgNCs 表现出非常高的猝灭效率,为低检测限 33.4 fM 的超灵敏检测铺平了道路。特别是,该策略在检测靶 miRNA-155 对对照 miRNA 的检测中表现出优异的特异性和选择性,包括突变 miRNA-155、miRNA-21、miRNA-141、let-7a 和 miRNA-182。此外,通过对临床血清样本中 miRNA-155 表达水平的评估,证实了该系统的实际应用价值,结果令人满意,表明该传感平台有望应用于疾病诊断以及生物化学的基础研究。

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