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基于电动力学不稳定性的低成本、无标记 DNA 检测方法,在长距离 PCR 中的应用。

A low-cost, label-free DNA detection method in lab-on-chip format based on electrohydrodynamic instabilities, with application to long-range PCR.

机构信息

UMR 168 Institut Curie, Centre National de la Recherche Scientifique et Université Pierre et Marie Curie, 26 Rue d'Ulm, 75005, Paris, France.

出版信息

Lab Chip. 2012 Nov 21;12(22):4738-47. doi: 10.1039/c2lc40372b.

Abstract

In order to evolve from a "chip in the lab" to a "lab on a chip" paradigm, there is still a strong demand for low-cost, portable detection technologies, notably for analytes at low concentrations. Here we report a new label-free DNA detection method with direct electronic read, and apply it to long-range PCR. This method uses a nonlinear electrohydrodynamic phenomenon: when subjected to high electric fields (typically above 100 V cm(-1)), suspensions of large polyelectrolytes, such as long DNA molecules, create "giant" dynamic concentration fluctuations. These fluctuations are associated with large conductivity inhomogeneities, and we use here a contact-mode local conductivity detector to detect these fluctuations. In order to decouple the detection electronics from the high voltage excitation one, an original "doubly symmetric" floating mode battery-operated detection scheme was developed. A wavelet analysis was then applied, to unravel from the chaotic character of the electohydrodynamic instabilities a scalar signal robustly reflecting the amplification of DNA. As a first proof of concept, we measured the products of the off-chip amplification of 10 kbp DNA from lambda phage DNA, achieving a sensitivity better than 100 fg DNA in the original 50 μl sample. This corresponds to the amplification products of less than 100 initial copies of target DNA. The companion enabling technologies developed to implement this new concept, i.e. the doubly symmetric contact conductivity detection and wavelet analysis, may also find various other applications in lab-on-chips.

摘要

为了将芯片从实验室发展为芯片实验室,仍然强烈需要低成本、便携式的检测技术,特别是用于检测低浓度分析物的技术。在这里,我们报告了一种新的无标记 DNA 检测方法,具有直接的电子读取功能,并将其应用于长距离 PCR。该方法利用非线性电动力学现象:当处于高电场(通常超过 100 V cm(-1))时,大聚电解质(如长 DNA 分子)的悬浮液会产生“巨大”的动态浓度波动。这些波动与大的电导率非均匀性有关,我们在这里使用接触模式局部电导率检测器来检测这些波动。为了将检测电子设备与高压激励电子设备解耦,开发了一种原始的“双对称”浮动模式电池操作检测方案。然后应用小波分析,从电动力学不稳定性的混沌特征中解耦出一个稳健地反映 DNA 放大的标量信号。作为概念验证的第一步,我们测量了来自 lambda 噬菌体 DNA 的 10 kbp DNA 的离片扩增产物,在原始 50 μl 样品中实现了优于 100 fg DNA 的灵敏度。这对应于目标 DNA 的初始拷贝数小于 100 的扩增产物。为实现这一新概念而开发的配套使能技术,即双对称接触电导率检测和小波分析,也可能在芯片实验室中找到各种其他应用。

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