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

机译:用于核酸高敏感荧光检测的双信号放大策略

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摘要

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 targettriggered 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 AuNPtrefoil 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-re
机译:开发方便的感测探针和对生物分子的高敏感和特异性检测的策略对于疾病的诊断非常重要。这里,设计了具有目标触发的再循环和双链体核酸酶(DSN)介导的扩增的双信号放大策略并提出用于核酸的高敏感荧光测定。在该策略中,设计了三种特殊发夹结构的单链DNA(即,H1,H 2和H3),在靶DNA的存在下,在H1修饰的AUNPS(即AUNP-H1探针)上操作靶梗回收率和H3在AUNPS上形成三轴DNA(即,AUNP-TREFOIL)。然后将DSN与AuNPtrefeil一起孵育以切割双链三轴DNA,使标记在H 2和H 3上标记的ROX分子脱落,这导致回收ROx的先前AUNP淬火荧光信号。通过聚丙烯酰胺凝胶电泳和荧光表征证实了传感机制,并从几个方面进行了优化的感测策略,例如AUNP-H1探针(20分钟)和浓度(0.3u)和固定时间的MCH阻断时间( 15分钟)DSN。通过人血清中靶DNA的荧光测定研究了探针和双信号放大策略的实用性。获得从50 fm至100pm的良好线性校准曲线,低检测限为47.68 fm。感测策略表现出良好的特异性,可以有效地将靶DNA与单碱错配(SM)和完全无与伦比(UM)DNA的分解。恢复值从91.85%到106.3%的相对标准偏差(RSD)少于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探针和双信号放大策略提供了高效的诊断剂和分析疾病 - RE的方法

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  • 作者单位

    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 &

    Tel;

    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 &

    Tel;

    School of Geography and Biological Information Nanjing University of Posts &

    Telecommunications Nanjing 210023 China;

    School of Geography and Biological Information Nanjing University of Posts &

    Telecommunications Nanjing 210023 China;

    School of Geography and Biological Information Nanjing University of Posts &

    Telecommunications Nanjing 210023 China;

    Institute of Nano Biomedicine and Engineering Department of Instrument Science and Engineering Thin Film and Microfabrciation Key Laboratory of Administration of Education School of Electronic Information and Electrical Engineering Shanghai Jiao Tong;

    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 &

    Tel;

    School of Geography and Biological Information Nanjing University of Posts &

    Telecommunications Nanjing 210023 China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分析化学;
  • 关键词

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

    机译:双信号放大;高敏感的策略;核酸的荧光检测;

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