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A micropatterned substrate for on-surface enzymatic labelling of linearized long DNA molecules

机译:一种微图案化的底物用于表面酶标记线性化的长DNA分子

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摘要

Optical mapping of linearized DNA molecules is a promising new technology for sequence assembly and scaffolding, large structural variant detection, and diagnostics. This is currently achieved either using nanochannel confinement or by stretching single DNA molecules on a solid surface. While the first method necessitates DNA labelling before linearization, the latter allows for modification post-linearization, thereby affording increased process flexibility. Each method is constrained by various physical and chemical limitations. One of the most common techniques for linearization of DNA uses a hydrophobic surface and a receding meniscus, termed molecular combing. Here, we report the development of a microfabricated surface that can not only comb the DNA molecules efficiently but also provides for sequence-specific enzymatic fluorescent DNA labelling. By modifying a glass surface with two contrasting functionalities, such that DNA binds selectively to one of the two regions, we can control DNA extension, which is known to be critical for sequence-recognition by an enzyme. Moreover, the surface modification provides enzymatic access to the DNA backbone, as well as minimizing non-specific fluorescent dye adsorption. These enhancements make the designed surface suitable for large-scale and high-resolution single DNA molecule studies.
机译:线性化DNA分子的光学作图是用于序列组装和支架,大结构变异检测和诊断的有前途的新技术。目前,这是通过使用纳米通道限制或通过在固体表面上拉伸单个DNA分子来实现的。第一种方法需要在线性化之前进行DNA标记,而后一种方法则允许线性化后进行修饰,从而提高了处理的灵活性。每种方法都受到各种物理和化学限制的约束。 DNA线性化最常用的技术之一是使用疏水性表面和后退弯月面(称为分子梳)。在这里,我们报告了微加工表面的发展,该表面不仅可以有效地梳理DNA分子,而且还可以提供序列特异性酶促荧光DNA标记。通过修饰具有两个相反功能的玻璃表面,使DNA选择性结合到两个区域之一,我们可以控制DNA延伸,这对于酶识别序列至关重要。而且,表面修饰提供了酶促进入DNA骨架的通道,并最大程度地减少了非特异性荧光染料的吸附。这些增强使设计的表面适合大规模和高分辨率单DNA分子研究。

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