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一种用于核酸高灵敏荧光检测的双重信号放大策略。

A dual signal amplification strategy for the highly sensitive fluorescence detection of nucleic acids.

机构信息

Key Laboratory for Organic Electronics and Information Displays & Jiangsu Key Laboratory for Biosensors, Institute of Advanced Materials (IAM), Jiangsu National Synergetic Innovation Center for Advanced Materials (SICAM), Nanjing University of Posts & Telecommunications, Nanjing 210023, China.

出版信息

Analyst. 2020 Feb 17;145(4):1219-1226. doi: 10.1039/c9an02183c.

Abstract

The development of convenient sensing probes and strategies for the highly sensitive and specific detection of biomolecules is greatly significant for the diagnosis of diseases. Herein, a dual signal amplification strategy comprising target-triggered recycling and duplex-specific nuclease (DSN)-mediated amplifications was designed and proposed for a highly sensitive fluorescence assay of nucleic acids. In this strategy, three special hairpin structured single-stranded DNAs (i.e., H1, H2 and H3) were designed, and target-triggered recycling was operated on H1-modified AuNPs (i.e., AuNP-H1 probes) in the presence of target DNA, H2 and H3 to form trefoil DNAs on AuNPs (i.e., AuNP-trefoil). DSN was then incubated with AuNP-trefoil to cleave the double-stranded trefoil DNAs, causing the ROX molecules labelled on H2 and H3 to fall off the AuNPs, which resulted in the recovery of the previous AuNP-quenched fluorescence signal of ROX. The sensing mechanism was confirmed by polyacrylamide gel electrophoresis and fluorescence characterizations, and the sensing strategy was optimized from several aspects, such as the MCH blocking time of the AuNP-H1 probes (20 min) and the concentration (0.3 U) and immobilization time (15 min) of DSN. The practicability of the probes and the dual signal amplification strategy was investigated by a fluorescence assay of target DNA in human serum. A good linear calibration curve from 50 fM to 100 pM was obtained with a low detection limit of 47.68 fM. The sensing strategy showed good specificity, which could efficiently distinguish the target DNA from the single-base mismatched (SM) and completely unmatched (UM) DNAs. The recovery values ranging from 91.85% to 106.3% with the relative standard deviations (RSD) less than 7.30% also illustrated the good reliability of the proposed sensing probes and strategy. The AuNP-H1 probes and dual signal amplification strategy provide highly effective diagnostic agents and method for the analysis of disease-related nucleic acid biomarkers at the molecular level for early disease detection.

摘要

便捷感测探针的发展和生物分子高灵敏度、特异性检测的策略对于疾病的诊断具有重要意义。在此,设计并提出了一种包含目标触发循环和双链特异性核酸酶(DSN)介导的扩增的双重信号放大策略,用于核酸的高灵敏度荧光分析。在该策略中,设计了三种特殊的发夹结构单链 DNA(即 H1、H2 和 H3),并且在存在靶 DNA、H2 和 H3 的情况下,在 H1 修饰的金纳米颗粒(即 AuNP-H1 探针)上进行目标触发循环,以在 AuNPs 上形成三叶 DNA(即 AuNP-trefoil)。然后,将 DSN 与 AuNP-trefoil 孵育以切割双链三叶 DNA,导致标记在 H2 和 H3 上的 ROX 分子从 AuNPs 上脱落,从而恢复以前的 AuNP 猝灭的 ROX 荧光信号。通过聚丙烯酰胺凝胶电泳和荧光特性证实了传感机制,并从多个方面优化了传感策略,例如 AuNP-H1 探针的 MCH 阻断时间(20 分钟)和 DSN 的浓度(0.3 U)和固定时间(15 分钟)。通过在人血清中靶 DNA 的荧光分析研究了探针和双重信号放大策略的实用性。从 50 fM 到 100 pM 获得了良好的线性校准曲线,检测限低至 47.68 fM。该传感策略具有良好的特异性,能够有效地将靶 DNA 与单碱基错配(SM)和完全不匹配(UM)DNA 区分开。回收率范围为 91.85%至 106.3%,相对标准偏差(RSD)小于 7.30%,也说明了所提出的传感探针和策略的良好可靠性。AuNP-H1 探针和双重信号放大策略为分子水平上疾病相关核酸生物标志物的分析提供了高效的诊断试剂和方法,用于早期疾病检测。

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