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基于上转换纳米粒子的双识别步骤的荧光共振能量转移(LRET)用于 microRNAs 的单步、均相和灵敏检测。

Single-step, homogeneous and sensitive detection for microRNAs with dual-recognition steps based on luminescence resonance energy transfer (LRET) using upconversion nanoparticles.

机构信息

School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, Jiangsu 210023, PR China; Jiangsu Key Laboratory for Functional Substance of Chinese Medicine State Key Laboratory Cultivation Base for TCM Quality and Efficacy, Nanjing 210023, PR China.

School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, Jiangsu 210023, PR China.

出版信息

Biosens Bioelectron. 2018 Feb 15;100:475-481. doi: 10.1016/j.bios.2017.09.039. Epub 2017 Sep 22.

DOI:10.1016/j.bios.2017.09.039
PMID:28963965
Abstract

A single-step, homogeneous and sensitive LRET assay is presented for the detection of miRNAs. The amplification-free assay provides a unique combination of high specificity with dual-recognition approach of different hybridization and ligation steps and preventing background auto-fluorescence in biological samples using upconversion nanoparticles (UCNPs) as signal-producing nanoprobes. The assay probe is composed of signal-producing unit (a pair of homogeneous upconversion luminescence resonance energy transfer (UC-LRET)-based oligonucleotides) and recognition unit (two adaptor oligonucleotides). In the presence of target miRNAs, the probe and target miRNAs leads to the formation of stable double-strands and semi-stable adaptor-miRNAs complexes with an adaptor nick. Ligation of the nick using ligase cause the formation of stable double-strands, resulting in UCNPs-to-dye UC-LRET for detection of the miRNAs with near-infrared radiation (980nm). Sensitive detection of miRNA-21 at concentrations of 200pM to 1.4nM and detection limits of 0.095nM with good precision of 3.9% (RSD) for seven repeated measurements of 500pM miRNAs demonstrate the feasibility of both high throughput and point-of-care clinical diagnostics. The homogeneous UC-LRET assay without any washing can be extended to the application in other important types of nucleic acid analysis.

摘要

本文提出了一种用于 miRNA 检测的单步、均相和敏感的 LRET 分析方法。该无扩增检测法提供了高特异性的独特组合,采用不同杂交和连接步骤的双重识别方法,并利用上转换纳米粒子(UCNP)作为信号产生纳米探针来防止生物样品中的背景自荧光。该检测探针由信号产生单元(一对均相上转换发光共振能量转移(UC-LRET)基寡核苷酸)和识别单元(两个适配体寡核苷酸)组成。在存在靶 miRNA 的情况下,探针和靶 miRNA 导致形成稳定的双链体和具有适配体缺口的半稳定适配体-miRNA 复合物。使用连接酶连接缺口导致稳定双链体的形成,从而导致 UCNP 到染料的 UC-LRET,用于检测近红外辐射(980nm)下的 miRNA。在 200pM 至 1.4nM 的浓度下对 miRNA-21 进行敏感检测,检测限为 0.095nM,对 500pM miRNA 进行 7 次重复测量的精度为 3.9%(RSD),证明了高通量和即时临床诊断的可行性。无需任何洗涤的均相 UC-LRET 分析方法可扩展到其他重要类型的核酸分析应用中。

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