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首页> 外文期刊>Spectrochimica acta, Part A. Molecular and biomolecular spectroscopy >Label-free and enzyme-free one-step rapid colorimetric detection of DNA methylation based on unmodified gold nanoparticles
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Label-free and enzyme-free one-step rapid colorimetric detection of DNA methylation based on unmodified gold nanoparticles

机译:基于未修饰的金纳米粒子的无标记和酶无一步的DNA甲基化的无标记和一步的快速比色度检测

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DNA methylation has been identified as one of the important causes of tumorigenesis, so it is important to develop some advanced methods for detecting and quantifying DNA methylation. In this study, a label-free and enzyme-free one-step rapid colorimetric detection of DNA methylation based on unmodified Au nanoparticles (Au NPs)has been proposed. This method can quickly, efficiently, economically and easily colorimetric detect methylated DNA only by the color change of unmodified Au NPs solution without the covalent modification of Au NPs in advance or complicated instruments for implementation with practical limitations or expensive biological enzymes or traditional organic dyes during the reaction. The strategy employed the difference in electrostatic attraction of single-stranded DNA and double-stranded DNA against salt-induced aggregation of Au NPs. The method has a DNA methylated detection limit of 8.47 nM and it is distinctly visible to detect methylated DNA with the naked eye as low as 20 nM. Furthermore, the strategy has an ability to detect methylated DNA in the presence of abundant unmethylated DNA with the detection limit of 0.13% and as low as 1% methylated DNA can be distinguished in heterogeneous samples with the naked eye. Also, the stratagem provides a convenient and rapid platform for methylated DNA detection of human serum samples in one step, which displays a huge potential for clinical diagnosis and treatment of oncological diseases. (C) 2020 Elsevier B.V. All rights reserved.
机译:DNA甲基化已被鉴定为肿瘤发生的重要原因之一,因此可以制定一些用于检测和定量DNA甲基化的先进方法是重要的。在该研究中,已经提出了基于未修饰的Au纳米颗粒(Au nps)的DNA甲基化的无标记和无酶的一步的快速比色度检测。该方法只能通过未修饰的Au NPS溶液的颜色变化快速,高效地,经济,易于比色测量甲基化DNA,而无需预先改变Au NP或复杂的仪器,用于实施具有实际限制或昂贵的生物酶或传统的有机染料期间反应。该策略采用单链DNA和双链DNA静电吸引的差异,对Au nps的盐诱导的聚集。该方法具有8.47nm的DNA甲基化检测限,并且可以明显地检测与肉眼低至20nm的甲基化DNA。此外,该策略能够在大量未甲基化DNA存在下检测甲基化DNA,检测限为0.13%,低至1%甲基化DNA可以在与肉眼的异质样品中区分开。此外,Stratagem在一步中为人血清样品的甲基化DNA检测提供了方便快速的平台,这表达了临床诊断和肿瘤疾病治疗的巨大潜力。 (c)2020 Elsevier B.v.保留所有权利。

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