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Mechanisms of DNA separation in entropic trap arrays: A Brownian dynamics simulation

机译:熵陷阱阵列中DNA分离的机制:布朗动力学模拟

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摘要

Using Brownian dynamics simulations, we study the migration of long charged chains in an electrophoretic microchannel device consisting of an array of microscopic entropic traps with alternating deep regions and narrow constrictions. Such a device has been designed and fabricated recently by Han et al. for the separation of DNA molecules (Science, 2000). Our simulation reproduces the experimental observation that the mobility increases with the length of the DNA. A detailed data analysis allows to identify the reasons for this behavior. Two distinct mechanisms contribute to slowing down shorter chains. One has been described earlier by Han et al.: the chains are delayed at the entrance of the constriction and escape with a rate that increases with chain length. The other, actually dominating mechanism is here reported for the first time: Some chains diffuse out of their main path into the corners of the box, where they remain trapped for a long time. The probability that this happens increases with the diffusion constant, i.e., the inverse chain length.
机译:使用布朗动力学模拟,我们研究了电泳微通道设备中长电荷链的迁移,该设备由一系列交替排列的深区和狭窄收缩的微观熵阱组成。 Han等人最近已经设计和制造了这种装置。用于分离DNA分子(科学,2000年)。我们的模拟再现了实验观察,即迁移率随DNA的长度增加而增加。进行详细的数据分析可以确定这种现象的原因。有两种不同的机制有助于减慢较短的链。 Han等人早些时候已经描述了一种:链条在收缩部的入口处延迟并以随着链条长度增加的速率逸出。首次报道了另一个实际上占主导地位的机制:一些链条从其主要路径扩散到盒子的各个角落,在那里它们长时间被困住。发生这种情况的可能性随着扩散常数即逆链长而增加。

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