Deen Jochem, Sempels Wouter, De Dier Raf, Vermant Jan, Dedecker Peter, Hofkens Johan, Neely Robert K
Department of Chemistry, KU Leuven , Celestijnenlaan 200F, Heverlee 3001, Belgium.
ACS Nano. 2015 Jan 27;9(1):809-16. doi: 10.1021/nn5063497. Epub 2015 Jan 8.
Deposition of linear DNA molecules is a critical step in many single-molecule genomic approaches including DNA mapping, fiber-FISH, and several emerging sequencing technologies. In the ideal situation, the DNA that is deposited for these experiments is absolutely linear and uniformly stretched, thereby enabling accurate distance measurements. However, this is rarely the case, and furthermore, current approaches for the capture and linearization of DNA on a surface tend to require complex surface preparation and large amounts of starting material to achieve genomic-scale mapping. This makes them technically demanding and prevents their application in emerging fields of genomics, such as single-cell based analyses. Here we describe a simple and extremely efficient approach to the deposition and linearization of genomic DNA molecules. We employ droplets containing as little as tens of picograms of material and simply drag them, using a pipet tip, over a polymer-coated coverslip. In this report we highlight one particular polymer, Zeonex, which is remarkably efficient at capturing DNA. We characterize the method of DNA capture on the Zeonex surface and find that the use of droplets greatly facilitates the efficient deposition of DNA. This is the result of a circulating flow in the droplet that maintains a high DNA concentration at the interface of the surface/solution. Overall, our approach provides an accessible route to the study of genomic structural variation from samples containing no more than a handful of cells.
线性DNA分子的沉积是许多单分子基因组方法中的关键步骤,包括DNA图谱绘制、纤维荧光原位杂交(fiber-FISH)以及几种新兴的测序技术。在理想情况下,为这些实验沉积的DNA是绝对线性且均匀拉伸的,从而能够进行精确的距离测量。然而,实际情况很少如此,而且目前在表面捕获和线性化DNA的方法往往需要复杂的表面处理和大量的起始材料才能实现基因组规模的图谱绘制。这使得它们在技术上要求很高,并阻碍了它们在基因组学新兴领域(如单细胞分析)中的应用。在此,我们描述了一种简单且极其高效的基因组DNA分子沉积和线性化方法。我们使用含有低至几十皮克材料的液滴,并使用移液器吸头在聚合物涂层盖玻片上简单地拖动它们。在本报告中,我们重点介绍了一种特殊的聚合物——Zeonex,它在捕获DNA方面非常高效。我们对在Zeonex表面捕获DNA的方法进行了表征,发现使用液滴极大地促进了DNA的有效沉积。这是液滴中循环流动的结果,该流动在表面/溶液界面处维持了高DNA浓度。总体而言,我们的方法为研究来自不超过少数细胞的样本中的基因组结构变异提供了一条可行途径。