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首页> 外文期刊>Analytica chimica acta >Ultrasensitive detection of microRNA based on a homogeneous label-free electrochemical platform using G-triplex/methylene blue as a signal generator
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Ultrasensitive detection of microRNA based on a homogeneous label-free electrochemical platform using G-triplex/methylene blue as a signal generator

机译:基于均匀的无标签电化学平台的微小RORNA使用G-Triple /亚甲基蓝色作为信号发生器的超声检测

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The electrochemical methods for microRNA (miRNA) detection have received increasing attention because high portability and affordability of electrochemical biosensors may facilitate point-of-care quantitative detection of miRNAs. Among these biosensors, the homogenous label-free electrochemical biosensors for miRNAs are rarely reported due to the lack of a universal and efficient signal read-out-mode. A newly discovered G-triplex, 5'-CTGGGAGGGAGGGA-3' (denoted as G3), can specifically bind with methylene blue (MB), leading to a significant decrease of the diffusion current of MB. By using miRNAs as a driving force, a two-stage isothermal exponential amplification reaction was proposed to generate G3 through miRNAs. The generated G3 can combine with MB and produce observable current changes, which depend on the concentration of miRNAs. Therefore, a novel homogeneous label-free electrochemical biosensor for miRNA detection was successfully constructed. By choosing let-7a, the down-regulation of which is possibly associated with the over-expression of RAS and HMGA2 oncogenes, as a model, we discovered that this biosensor demonstrated excellent analytical performance in detecting let-7a, with an ultralow limit of detection (0.45 fM) and high specificity (discriminating one nucleotide variation). Moreover, the proposed biosensor was successfully applied in monitoring the expression levels of the low-abundant miRNAs in the human lung adenocarcinoma cell lines. This assay successfully verified the feasibility of G-triplex/MB as an efficient and sensitive probe for immobilization-free and label-free electrochemical detection of nucleic acids, which would greatly promote the rapid development of homogeneous label-free electrochemical biosensors. (C) 2020 Elsevier B.V. All rights reserved.
机译:微小RORNA(miRNA)检测的电化学方法已经得到了越来越多的关注,因为电化学生物传感器的高便携性和可承受能力可以促进MIRNA的护理点定量检测。在这些生物传感器中,由于缺乏通用和有效的信号读出模式,很少报道MIRNA的均相无均匀的无标记电化学生物传感器。新发现的G-Triplex,5'-CtGGGagGGGGGGGA-3'(表示为G3),可以与亚甲基蓝(MB)特异性结合,导致MB的扩散电流的显着降低。通过使用MiRNA作为驱动力,提出了一种两级等温指数扩增反应,以通过miRNA产生G3。所生成的G3可以与MB组合并产生可观察电流变化,这取决于miRNA的浓度。因此,成功构建了用于miRNA检测的新型均匀的无标记电化学生物传感器。通过选择Let-7a,其下调可能与RAS和HMGA2癌基因的过表达相关,作为模型,我们发现这种生物传感器在检测Let-7a中表现出优异的分析性能,具有超极限检测(0.45 fm)和高特异性(鉴别一个核苷酸变异)。此外,所提出的生物传感器被成功地应用于监测人肺腺癌细胞系中低丰富miRNA的表达水平。该测定成功地验证了G-Triplex / Mb的可行性作为用于无致固化和无标签的核酸的无标记电化学检测的有效和敏感的探针,这将极大地促进无均匀的无标记电化学生物传感器的快速发展。 (c)2020 Elsevier B.V.保留所有权利。

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