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Highly Sensitive Multiple microRNA Detection Based on Fluorescence Quenching of Graphene Oxide and Isothermal Strand-Displacement Polymerase Reaction

机译:基于氧化石墨烯的荧光猝灭和等温链置换聚合酶反应的高灵敏多重microRNA检测

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摘要

A simple, highly sensitive, and selective multiple microRNA (miRNA) detection method based on the graphene oxide (GO) fluorescence quenching and isothermal strand-displacement polymerase reaction (ISDPR) was proposed. The capability to discriminate ssDNA and double-stranded nucleic acid structure coupled with the extraordinary fluorescence quenching of GO on multiple organic dye allows the proposed strategy to simultaneously and selectively detect several miRNA labeled with different dyes in the same solution, while the ISDPR amplification endows the detection method with high sensitivity. The strong interaction between ssDNA and GO led to the fluorescent ssDNA probe exhibiting minimal background fluorescence. Upon the recognition of specific target miRNA, an ISDPR was triggered to produce numerous massive specific DNA-miRNA duplex helixes, and a strong emission was observed due to the weak interaction between the DNA-miRNA duplex helix and GO. A miRNA biosensor down to 2.1 fM with a linear range of 4 orders of magnitude was obtained. Furthermore, the large planar surface of GO allows simultaneous quenching of several DNA probes with different dyes and produces a multiple biosensing platform with high sensitivity and selectivity, which has promising application in profiling the pattern of miRNA expression and biomedical research.
机译:提出了一种基于氧化石墨烯(GO)荧光猝灭和等温链置换聚合酶反应(ISDPR)的简单,高灵敏度,选择性的多个microRNA(miRNA)检测方法。区分ssDNA和双链核酸结构的能力,以及在多种有机染料上对GO进行非凡的荧光淬灭,使得所提出的策略能够在同一溶液中同时并选择性地检测几种用不同染料标记的miRNA,而ISDPR扩增赋予了这种优势。检测方法灵敏度高。 ssDNA和GO之间的强相互作用导致荧光ssDNA探针显示出最小的背景荧光。一旦识别出特定的靶标miRNA,就会触发ISDPR产生大量大量的特异性DNA-miRNA双链螺旋,并且由于DNA-miRNA双链螺旋与GO之间的弱相互作用而观察到强发射。获得了线性范围为4个数量级的低至2.1 fM的miRNA生物传感器。此外,GO的大平面可以同时淬灭几种具有不同染料的DNA探针,并产生具有高灵敏度和选择性的多重生物传感平台,这在分析miRNA表达模式和生物医学研究方面具有广阔的应用前景。

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