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Fracture Fabrication of a Multi-scale Channel Device that Efficiently Captures and Linearizes DNA from Dilute Solutions

机译:有效捕获和线性化稀溶液中DNA的多尺度通道设备的断裂加工

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摘要

This paper describes a simple technique for patterning channels on elastomeric substrates, at two distinct scales of depth, through the use of controlled fracture. Control of channel depth is achieved by the careful use of different layers of PDMS, where the thickness and material properties of each layer, and the position of layers relative to one another, dictate the depth of the channels formed. The system created in this work consists of a single ‘deep’ channel, whose width can be adjusted between the micron- and nano-scale by the controlled application or removal of a uniaxial strain, and an array of ‘shallow’ nano-scale channels oriented perpendicular to the ‘deep’ channel. The utility of this system is demonstrated through the successful capture and linearization of DNA from a dilute solution, by executing a two-step ‘concentrate-then-linearize’ procedure. When the ‘deep’ channel is in its open state, and a voltage is applied across the channel network, an overlapping electric double layer forms within the ‘shallow’ channel array. This overlapping electric double layer is used to prevent passage of DNA into the ‘shallow’ channels when the DNA molecules migrate into the junctional region by electrophoresis. Release of the applied strain then allows the ‘deep’ channel to return to its closed state, reducing the cross-sectional area of this channel from the micro- to the nano-scale. The resulting hydrodynamic flow and nano-confinement effects then combine to efficiently uncoil and trap the DNA in its linearized form. By adopting this strategy, we were able to overcome the entropic barriers associated with capturing and linearizing DNA derived from a dilute solution.
机译:本文介绍了一种通过使用受控断裂在两个不同的深度尺度上在弹性体基材上构图通道的简单技术。通道深度的控制是通过谨慎使用PDMS的不同层来实现的,其中每一层的厚度和材料属性以及各层相对于彼此的位置决定了所形成通道的深度。在这项工作中创建的系统由单个“深”通道和一系列“浅”纳米级通道组成,该通道的宽度可以通过受控施加或去除单轴应变在微米和纳米级之间进行调节。垂直于“深”通道定向。通过执行两步“浓缩-然后-线性化”程序,成功地从稀溶液中捕获和线性化了DNA,证明了该系统的实用性。当“深”通道处于打开状态,并且在通道网络上施加电压时,“浅”通道阵列中会形成一个重叠的双电层。当DNA分子通过电泳迁移到连接区时,这种重叠的双电层可防止DNA进入“浅”通道。然后释放所施加的应变可以使“深”通道返回其关闭状态,从而将该通道的横截面积从微米级减小到纳米级。然后,所产生的流体动力流和纳米约束效应相结合,可以有效地解开并捕获线性化形式的DNA。通过采用这种策略,我们能够克服与捕获和线性化源自稀溶液的DNA相关的熵障碍。

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