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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Label-free fluorescence strategy for sensitive microRNA detection based on isothermal exponential amplification and graphene oxide
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Label-free fluorescence strategy for sensitive microRNA detection based on isothermal exponential amplification and graphene oxide

机译:基于等温指数扩增和氧化石墨烯的灵敏microRNA检测的无标记荧光策略

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摘要

MicroRNAs (miRNAs) play an important role in many biological processes, and have been regarded as potential targets and biomarkers in cancer diagnosis and therapy. Also, to meet the big challenge imposed by the characteristics of miRNAs, such as small size and vulnerability to enzymatic digestion, it is of great importance to develop accurate, sensitive and simple miRNA assays. Herein, we developed a label-free fluorescence strategy for sensitive miRNA detection by combining isothermal exponential amplification and the unique features of SYBR Green I (SG) and graphene oxide (GO), in which SG gives significantly enhanced fluorescence upon intercalation into double-stranded DNAs (dsDNAs), and GO selectively adsorbs miRNA, single-stranded DNA and SG, to protect miRNA from enzymatic digestion, and to quench the fluorescence of the adsorbed SG. In the presence of the target miRNA, the ingeniously designed hairpin probe (HP) is unfolded and the subsequent polymerization and strand displacement reaction takes place to initiate the target recycling process. The newly formed dsDNAs are then recognized and cleaved by the nicking enzyme, generating new DNA triggers with the same sequence as the target miRNA, which hybridize with intact HPs to initiate new extension reactions. As a result, the circular exponential amplification for target miRNA is achieved and large amount of dsDNAs are formed to generate significantly enhanced fluorescence upon the intercalation of SG. Thus sensitive and selective fluorescence miRNA detection is realized, and the detection limit of 3 fM is obtained. Besides, this method exhibits additional advantages of simplicity and low cost, since expensive and tedious labeling process is avoided. Therefore, the as-proposed label-free fluorescence strategy has great potential in the applications in miRNA-related clinical practices and biochemical researches. (C) 2015 Elsevier B.V. All rights reserved.
机译:微小RNA(miRNA)在许多生物学过程中都起着重要作用,并已被视为癌症诊断和治疗中的潜在靶标和生物标记。同样,为了应对miRNA特性所带来的巨大挑战,例如体积小和易受酶消化的影响,开发准确,灵敏和简单的miRNA检测方法也非常重要。在本文中,我们通过结合等温指数扩增以及SYBR Green I(SG)和氧化石墨烯(GO)的独特功能,开发了一种用于敏感miRNA检测的无标记荧光策略,其中SG在插入双链时显着增强了荧光DNA(dsDNA)和GO选择性吸附miRNA,单链DNA和SG,以保护miRNA免受酶消化,并淬灭吸附的SG的荧光。在目标miRNA的存在下,精心设计的发夹探针(HP)展开,随后发生聚合反应和链置换反应,以启动目标回收过程。然后,新形成的dsDNA被切刻酶识别并切割,从而产生具有与靶标miRNA相同序列的新DNA触发信号,并与完整的HP杂交以引发新的延伸反应。结果,实现了目标miRNA的环状指数扩增,并形成大量dsDNA,从而在SG插入时产生显着增强的荧光。这样就实现了灵敏和选择性的荧光miRNA检测,并获得了3 fM的检测限。此外,由于避免了昂贵且乏味的标记过程,该方法还具有简单和低成本的优点。因此,提出的无标记荧光策略在与miRNA相关的临床实践和生化研究中的应用具有巨大潜力。 (C)2015 Elsevier B.V.保留所有权利。

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