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首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Simple, sensitive and label-free electrochemical detection of microRNAs based on the in situ formation of silver nanoparticles aggregates for signal amplification
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Simple, sensitive and label-free electrochemical detection of microRNAs based on the in situ formation of silver nanoparticles aggregates for signal amplification

机译:基于原位形成的银纳米颗粒聚集体的简单,灵敏和无标记的电化学检测用于信号放大

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This work presented a simple, sensitive and label-free electrochemical method for the detection of microRNAs (miRNAs). It is based on the boronate ester covalent interaction between 4-mercaptophenylboronic acid (MPBA) and cis-diol at the 3'-terminal of miRNAs and the MPBA-induced in situ formation of citrate-capped silver nanoparticles (AgNPs) aggregates as labels on the electrode surface. In this design, MPBA acted as the cross-linker of AgNPs assembly. Specifically, the thiolated hairpin-like DNA probe was assembled onto the gold nanoparticles (nano-Au) modified electrode surface through the Ag-S interaction. After hybridization with the target miRNAs, MPBA was anchored onto the 3'-terminal of miRNAs through the formation of a boronate ester bond and then captured AgNP via the Ag-S interaction. Meanwhile, free MPBA molecules in solution induced the in situ assembly of AgNPs on electrode surface through the covalent interactions between a-hydroxycarboxylate of citrate and boronate of MPBA and the formation of Ag-S bonds. The electrochemical signal was therefore amplified due to the formation of AgNPs network architecture. To demonstrate the feasibility and analytical performances of the method, miRNA-21 was determined as a model analyte. The detection limit was found to be 20 aM. The viability of our method for biological sample assays was demonstrated by measuring the miRNA-21 contents in three human serum samples. In contrast to other signal-amplified electrochemical strategies for miRNAs detection, our method requires simple detection principle and easy operation procedure and obviates the specific modification of nanoparticles and capture/detection probes.
机译:这项工作提出了一种简单,灵敏和无标记的无电化学方法,用于检测MicroRNA(miRNA)。它基于MiRNA的3'-末端的4-巯基苯基硼酸(MPBA)和CIS-DIOL之间的硼酸酯共价相互作用,并在原位形成柠檬酸封端的银纳米颗粒(AgNP)聚集体作为标签电极表面。在这种设计中,MPBA充当了AGNPS组件的交联剂。具体地,通过AG-S相互作用组装硫醇型发夹样DNA探针在金纳米颗粒(纳米-AU)修饰的电极表面上。在用靶miRNA杂交之后,通过形成硼酸酯键并通过AG-S相互作用捕获AGNP,将MPBA锚定到MIRNA的3'-末端。同时,通过柠檬酸盐和MPBA的柠檬酸氢甲酸氢酸酯与MPBA的硼酸盐之间的共价相互作用和AG-S键的形成,在溶液中诱导溶液中AgNP的原位组装在电极表面上。因此,由于AGNPS网络架构的形成,因此放大了电化学信号。为了证明该方法的可行性和分析性能,MiRNA-21被确定为模型分析物。发现检测限为20 AM。通过在三种人血清样品中测量miRNA-21含量来证明我们的生物样品测定方法的可行性。与MiRNA检测的其他信号放大的电化学策略相反,我们的方法需要简单的检测原理和易于操作程序,并且避免了纳米颗粒的特异性修饰和捕获/检测探针。

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