School of Life Science, and ‡School of Chemistry and Materials Science, Jiangsu Normal University , Xuzhou 221116, China.
Anal Chem. 2018 Jan 16;90(2):1098-1103. doi: 10.1021/acs.analchem.7b01991. Epub 2017 Dec 21.
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.
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。