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Electrode-Free Concentration and Recovery of DNA at Physiologically Relevant Ionic Concentrations

机译:在生理相关离子浓度下,无电极浓度和DNA的回收率

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摘要

Advances in microanalytical and microfluidic technologies have enabled rapid and amplification-free detection of DNA with a high signal-to-noise ratio. The low sample volume, however, poses a limit in the DNA detection sensitivity, which can be challenging for analyzing rare DNA in physiological samples. One way to improve the sensitivity is to concentrate the DNA in the sample prior to the analysis. The most common DNA concentration techniques are based on electrokinetics, which require an external electric field and generally become ineffective in high ionic concentration conditions. In this work, we present a facile method termed high-salt molecular rheotaxis (HiSMRT) to concentrate and recover DNA from samples with physiologically relevant ionic concentrations without any external electric field. HiSMRT requires only pressure-driven flow and ion concentration gradient to induce a stable local electric field and achieve DNA concentration, making it impervious to high ionic concentrations. We demonstrate that HiSMRT performs robustly at ionic concentrations equivalent to 2%-20% of the ionic concentration in blood serum. HiSMRT can concentrate DNA by up to 960-fold and recover an average of 96.4% of the DNA fragments from 2.0 to 23 kbp uniformly. The concentration process using HiSMRT takes as little as 7.5 min. Moreover, we show that this technique can be easily integrated to perform DNA concentration, size separation, and single-molecule detection all in one platform. We anticipate that this technique will be applicable to a wide range of biological samples and will help to improve the sensitivity of nucleic acid detection for low-abundance DNA biomarkers.
机译:微量分析和微流体技术的进展使得具有高信噪比的DNA的无快速和放大的检测。然而,低样品体积造成DNA检测灵敏度的极限,这可能是对分析生理样品中稀有DNA的挑战。提高敏感性的一种方法是在分析之前将DNA集中在样品中。最常见的DNA浓度技术基于电动性,其需要外部电磁场并且通常在高离子浓度条件下变得无效。在这项工作中,我们提出了一种归属化方法,称为高盐分子rheotaxis(Hismrt)以浓缩并从具有生理相关离子浓度的样品中浓缩和恢复DNA,而无需任何外部电场。 Hismrt仅需要压力驱动的流动和离子浓度梯度,以诱导稳定的局部电场并实现DNA浓度,使其不透水至高离子浓度。我们证明Hismrt在离子浓度下鲁棒地表现为相当于血液血清中离子浓度的2%-20%的离子浓度。 Hismrt可以将DNA浓缩至960倍,并均匀地从2.0至23kbp的平均DNA片段中恢复为96.4%。使用HISMRT的浓缩过程只需7.5分钟。此外,我们表明该技术可以容易地集成,以在一个平台中进行所有的DNA浓度,尺寸分离和单分子检测。我们预计该技术将适用于各种生物样品,并有助于提高低丰度DNA生物标志物的核酸检测的敏感性。

著录项

  • 来源
    《Analytical chemistry》 |2020年第8期|共8页
  • 作者单位

    Johns Hopkins Univ Dept Mech Engn Baltimore MD 21218 USA;

    Johns Hopkins Univ Dept Biomed Engn Baltimore MD 21218 USA;

    Johns Hopkins Univ Dept Mech Engn Baltimore MD 21218 USA;

    Johns Hopkins Univ Dept Biomed Engn Baltimore MD 21218 USA;

    Johns Hopkins Univ Dept Mech Engn Baltimore MD 21218 USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分析化学;
  • 关键词

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