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用于DNA甲基化密度高分辨率熔解分析的微滴阵列平台

Droplet Array Platform for High-Resolution Melt Analysis of DNA Methylation Density.

作者信息

Athamanolap Pornpat, Shin Dong Jin, Wang Tza-Huei

机构信息

Department of Biomedical Engineering, The Johns Hopkins University, Baltimore, MD, USA.

Department of Biomedical Engineering, The Johns Hopkins University, Baltimore, MD, USA Department of Mechanical Engineering, The Johns Hopkins University, Baltimore, MD, USA

出版信息

J Lab Autom. 2014 Jun;19(3):304-12. doi: 10.1177/2211068213507923. Epub 2013 Oct 10.

Abstract

High-resolution melting (HRM) has garnered significant interest as an analytical technique for a number of applications, including DNA methylation detection, due to its inherent sensitivity and robustness. In this study, we describe a miniaturized assay platform for quantitative methylation density analysis using a microfluidic droplet array cartridge. We demonstrate that the DNA methylation level of the RASSF1A promoter can be directly analyzed using HRM. PCR products were generated by amplifying bisulfite-treated DNA with varying CpG densities using CpG island-flanking primer sets. Subsequent HRM analysis on the miniaturized droplet platform shows distinct melting curve profiles associated with methylation levels, which was verified using a conventional benchtop PCR-HRM system. The characteristic melting temperature (Tm) of the PCR products was used to directly quantify the respective levels of DNA methylation density. Our approach provides a key advantage over current gold standard methods such as methylation-specific PCR (MSP), which are incapable of providing specific information regarding the overall methylation density of the target genes. The miniaturized platform establishes a practical approach to methylation density profiling from multiple DNA samples with a potential application in point-of-care diagnostics.

摘要

高分辨率熔解曲线分析(HRM)作为一种分析技术,因其固有的灵敏度和稳健性,在包括DNA甲基化检测在内的许多应用中引起了广泛关注。在本研究中,我们描述了一种使用微流控液滴阵列芯片进行定量甲基化密度分析的小型化检测平台。我们证明,可以使用HRM直接分析RASSF1A启动子的DNA甲基化水平。使用位于CpG岛侧翼的引物对,通过扩增经亚硫酸氢盐处理的具有不同CpG密度的DNA来生成PCR产物。随后在小型化液滴平台上进行的HRM分析显示出与甲基化水平相关的独特熔解曲线图谱,这通过传统的台式PCR-HRM系统得到了验证。PCR产物的特征熔解温度(Tm)用于直接定量DNA甲基化密度的各自水平。我们的方法相对于当前的金标准方法如甲基化特异性PCR(MSP)具有关键优势,后者无法提供有关靶基因总体甲基化密度的具体信息。该小型化平台建立了一种从多个DNA样本进行甲基化密度分析的实用方法,在即时诊断中具有潜在应用价值。

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