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基于金纳米粒子@硫化镉量子点原位相互作用及荧光共振能量转移机制,通过基于杂交链式反应的方法对Let-7a微小核糖核酸进行荧光检测。

Fluorescence-based detection of Let-7a miRNA through HCR-based approach upon the in situ interaction of AuNPs@CdS QDs and FRET mechanism.

作者信息

Hosseini Farid, Dadmehr Mehdi, Hosseini Morteza

机构信息

Department of Biology, Payame Noor University, Tehran, Iran.

Department of Life Science Engineering, Faculty of New Sciences & Technologies, University of Tehran, Tehran, Iran.

出版信息

Mikrochim Acta. 2025 Feb 12;192(3):153. doi: 10.1007/s00604-025-07018-y.

Abstract

A novel strategy is presented based on integration of nanostructures and molecular amplification was developed for detection of Let-7a miRNA as the carcinogenic cancer marker. Hybridization chain reaction (HCR) was triggered through the presence of Let-7a as the initiator target. This reaction resulted to the formation of AuNPs@CdS QDs assembly due to thiol bonding and following FRET occurred between free AuNPs and CdS QDs. Characterization and morphology of AuNPs@CdS QDs showed in situ accumulation of CdS QDs and afterward optical changes in fluorescence emission. The quenching of fluorescence emission was observed which corresponded  to Let-7a concentration in the linear range 10-45 pM with LOD of 2 pM. The sensitivity and selectivity of the performed study confirmed the efficiency of the proposed strategy. Additionally, it demonstrated a high level of specificity and detection performance in real-sample analysis.

摘要

提出了一种基于纳米结构整合和分子扩增的新策略,用于检测作为致癌癌症标志物的Let-7a微小RNA。通过存在Let-7a作为引发剂靶标来触发杂交链式反应(HCR)。由于硫醇键合,该反应导致形成AuNPs@CdS量子点组装体,随后在游离AuNPs和CdS量子点之间发生荧光共振能量转移(FRET)。AuNPs@CdS量子点的表征和形态显示CdS量子点的原位积累以及随后荧光发射的光学变化。观察到荧光发射猝灭,其对应于线性范围为10 - 45 pM的Let-7a浓度,检测限为2 pM。所进行研究的灵敏度和选择性证实了所提出策略的有效性。此外,它在实际样品分析中表现出高度的特异性和检测性能。

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