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 >MicroRNA detection based on duplex-specific nuclease-assisted target recycling and gold nanoparticle/graphene oxide nanocomposite-mediated electrocatalytic amplification
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MicroRNA detection based on duplex-specific nuclease-assisted target recycling and gold nanoparticle/graphene oxide nanocomposite-mediated electrocatalytic amplification

机译:基于双相特异性核酸酶辅助目标回收和金纳米颗粒/石墨烯氧化物纳米复合材料介导的电催化扩增的MicroRNA检测

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摘要

DNA technology based bio-responsive nanomaterials have been widely studied as promising tools for biomedical applications. Gold nanoparticles (AuNPs) and graphene oxide (GO) sheets are representative zero- and two-dimensional nanomaterials that have long been combined with DNA technology for point-of-care diagnostics. Herein, a cascade amplification system based on duplex-specific nuclease (DSN)-assisted target recycling and electrocatalytic water-splitting is demonstrated for the detection of microRNA. Target microRNAs can form DNA: RNA heteroduplexes with DNA probes on the surface of AuNPs, which can be hydrolyzed by DSN. MicroRNAs are preserved during the reaction and released into the suspension for the digestion of multiple DNA probes. After the DSN-based reaction, AuNPs are collected and mixed with GO to form AuNP/GO nanocomposite on an electrode for the following electrocatalytic amplification. The utilization of AuNP/GO nanocomposite offers large surface area, exceptional affinity to water molecules, and facilitated mass diffusion for the water-splitting reaction. For let-7b detection, the proposed biosensor achieved a limit detection of 1.5 fM in 80 min with a linear detection range of approximately four orders of magnitude. Moreover, it has the capability of discriminating non-target microRNAs containing even single-nucleotide mismatches, thus holding considerable potential for clinical diagnostics.
机译:基于DNA技术的生物响应纳米材料已被广泛研究为生物医学应用的有希望的工具。金纳米颗粒(AUNP)和石墨烯氧化物(GO)片材是代表性的零和二维纳米材料,其长期与DNA技术结合在护理点诊断。在此,证明了基于双相核酸酶(DSN)的核酸酶(DSN)的靶回收率和电催化水分解的级联扩增系统用于检测MicroRNA。靶微型鼠标可以形成DNA:RNA异疏细胞与AUNPS表面上的DNA探针,其可以通过DSN水解。在反应过程中保存微小RNA,并释放到悬浮液中以消化多个DNA探针。在基于DSN的反应之后,收集AUNP并将其混合在电极上形成AUNP / GO纳米复合材料,以进行以下电催化扩增。 AUNP / GO纳米复合材料的利用提供了大的表面积,对水分子的特殊亲和力,以及用于水分解反应的促进质量扩散。对于Let-7B检测,所提出的生物传感器在80分钟内实现了1.5 fm的极限检测,线性检测范围大约为四个数量级。此外,它具有鉴别含有甚至单核苷酸错配的非靶微米体的能力,从而保持临床诊断的相当潜力。

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