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样本自数字化(SD)芯片中的数字 LAMP。

Digital LAMP in a sample self-digitization (SD) chip.

机构信息

Department of Chemistry, University of Washington, Seattle, USA.

出版信息

Lab Chip. 2012 Jun 21;12(12):2247-54. doi: 10.1039/c2lc21247a. Epub 2012 Mar 7.

DOI:10.1039/c2lc21247a
PMID:22399016
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3383853/
Abstract

This paper describes the realization of digital loop-mediated DNA amplification (dLAMP) in a sample self-digitization (SD) chip. Digital DNA amplification has become an attractive technique to quantify absolute concentrations of DNA in a sample. While digital polymerase chain reaction is still the most widespread implementation, its use in resource-limited settings is impeded by the need for thermal cycling and robust temperature control. In such situations, isothermal protocols that can amplify DNA or RNA without thermal cycling are of great interest. Here, we accomplished the successful amplification of single DNA molecules in a stationary droplet array using isothermal digital loop-mediated DNA amplification. Unlike most (if not all) existing methods for sample discretization, our design allows for automated, loss-less digitization of sample volumes on-chip. We demonstrated accurate quantification of relative and absolute DNA concentrations with sample volumes of less than 2 μl. We assessed the homogeneity of droplet size during sample self-digitization in our device, and verified that the size variation was small enough such that straightforward counting of LAMP-active droplets sufficed for data analysis. We anticipate that the simplicity and robustness of our SD chip make it attractive as an inexpensive and easy-to-operate device for DNA amplification, for example in point-of-care settings.

摘要

本文描述了在样本自数字化(SD)芯片中实现数字环介导 DNA 扩增(dLAMP)。数字 DNA 扩增已成为定量样品中 DNA 绝对浓度的一种有吸引力的技术。虽然数字聚合酶链反应仍然是最广泛的应用,但由于需要热循环和稳健的温度控制,其在资源有限的环境中的应用受到阻碍。在这种情况下,无需热循环即可扩增 DNA 或 RNA 的等温协议非常有吸引力。在这里,我们使用等温数字环介导 DNA 扩增在固定液滴阵列中成功扩增了单个 DNA 分子。与大多数(如果不是全部)现有的样品离散化方法不同,我们的设计允许在芯片上自动、无损地对样品体积进行数字化。我们使用小于 2 μl 的样品体积证明了相对和绝对 DNA 浓度的准确定量。我们评估了我们的设备中样品自数字化过程中液滴大小的均匀性,并验证了大小变化足够小,以至于简单地计算 LAMP 活性液滴就足以进行数据分析。我们预计我们的 SD 芯片的简单性和稳健性使其成为一种廉价且易于操作的 DNA 扩增设备,例如在即时护理环境中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/363f/3383853/aa204e6576ab/nihms385240f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/363f/3383853/e4629b56d1a3/nihms385240f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/363f/3383853/b2eff3a5b7bf/nihms385240f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/363f/3383853/858772f8b495/nihms385240f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/363f/3383853/aa204e6576ab/nihms385240f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/363f/3383853/e4629b56d1a3/nihms385240f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/363f/3383853/b2eff3a5b7bf/nihms385240f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/363f/3383853/858772f8b495/nihms385240f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/363f/3383853/aa204e6576ab/nihms385240f4.jpg

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