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首页> 外文期刊>Analytical methods >Core-shell CdSeTe/ZnS quantum dots for the detection of microRNA-155 based on the fluorescence resonance energy transfer technique via the formation of a network structure
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Core-shell CdSeTe/ZnS quantum dots for the detection of microRNA-155 based on the fluorescence resonance energy transfer technique via the formation of a network structure

机译:基于荧光共振能量传递技术的网络结构,核壳CDSET / ZNS量子点用于检测MicroRNA-155

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摘要

The microRNA family shows great promise for the diagnosis and prediction of different cancers as biomarkers, in which miRNA-155 (miR155) is recognized as a biomarker for lung cancer and thus has drawn much attention. Therefore, the development of specific and accurate methods to detect miR155 has become a potential research hotspot. In this work, we presented a fluorescence resonance energy transfer (FRET) technique by utilizing core-shell CdSeTe/ZnS quantum dots (QDs) as a signal reporter and a target recycling strategy as a signal amplifier for the detection of miR155. In the presence of miR155, part of the hairpin probe (HP) immobilized onto the surface of gold nanoparticles (AuNPs)@SiO2, could hybridize with it. Then, numerous H1-AuNPs@SiO2 could be produced with the aid of exonuclease III. With the linkage of the assistant chain A2, H1-AuNPs@SiO2 combined with A1-QDs and then the fluorescence (FL) signal of QDs was quenched by AuNPs@SiO(2)via FRET. The more miR155 present in solution, the weaker the detected FL signal. A linear response range of 0.01 fM to 1 nM and low detection limit of 3 aM were obtained using the proposed method. Furthermore, this method showed high specificity and satisfactory recovery between 93 and 105% in real human serum samples, illustrating its great potential for practical applications.
机译:MicroRNA家族对诊断和预测不同癌症作为生物标志物的诊断和预测,其中MiRNA-155(MiR155)被认为是肺癌的生物标志物,因此引起了很多关注。因此,在检测MIR155检测MIR155的具体和准确方法的发展已成为潜在的研究热点。在这项工作中,我们通过利用核心壳CDSete / Zns量子点(QDS)作为信号报告器和作为用于检测MIR155的信号放大器的目标回收策略来呈现荧光共振能量转移(FRET)技术。在MiR155的存在下,将其固定在金纳米颗粒(AUNPS)的表面上的一部分发夹探针(HP)可以与其杂交。然后,可以借助于外切核酸酶III生产许多H1-AUNPS @ SiO 2。随着助剂链A2的连杆,H1-AUNPS @ SiO 2与A1-QD结合,然后通过FRER通过AUNPS @ SIO(2)淬灭QDS的荧光(FL)信号。溶液中存在的miR155越多,检测到的流动信号越弱。使用该方法获得了0.01 fm至1nm至3m的低检测限度的线性响应范围。此外,该方法在真正的人血清样品中显示出高93和105%的高特异性和令人满意的恢复,说明了其实际应用的巨大潜力。

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  • 来源
    《Analytical methods》 |2019年第32期|共9页
  • 作者单位

    Nanjing Tech Univ Coll Chem &

    Mol Engn Nanjing 211800 Jiangsu Peoples R China;

    Nanjing Tech Univ Coll Chem &

    Mol Engn Nanjing 211800 Jiangsu Peoples R China;

    Nanjing Tech Univ Coll Biotechnol &

    Pharmaceut Engn Nanjing 211800 Jiangsu Peoples R China;

    Nanjing Tech Univ Coll Chem &

    Mol Engn Nanjing 211800 Jiangsu Peoples R China;

    Nanjing Tech Univ Coll Chem &

    Mol Engn Nanjing 211800 Jiangsu Peoples R China;

    Nanjing Tech Univ Coll Chem &

    Mol Engn Nanjing 211800 Jiangsu Peoples R China;

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