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Agarose gel electrophoresis of DNA: A Brownian dynamics simulation.

机译:DNA的琼脂糖凝胶电泳:布朗动力学模拟。

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Agarose gel electrophoresis of DNA was investigated with a Brownian dynamics simulation. The terms in the Langevin equation, the equation of motion for the DNA chain, were selected to represent DNA and agarose as realistically as possible. The DNA was modeled as a bead-spring chain, and the agarose was modeled as a three dimensional array of regularly spaced cylindrical obstacles. Some simulations with randomly spaced and oriented obstacles were also completed. The simulation was able to duplicate much of the relevant experimental phenomena. The time averaged velocity in the simulation is a strongly decreasing function of chain length for shorter chains, but this dependence of velocity on chain length disappears for longer chain lengths. Investigation of the dynamic behavior of individual chains reveals that the motion of chains in the gel is characterized by a cycling of the chain between bunched and extended conformations. Moreover, this cycling occurs with a characteristic period which is dependent on the chain's contour length.; The response of chains to a sudden 120 degree change in field direction was investigated. Enhanced separation was predicted to occur in these pulsed field simulations. The increased resolution was due to a forced entanglement after field switching. The disentanglement is characterized by a disentanglement time which varies linearly with chain length. The disentanglement time and the conformational cycling period were found to be closely related with the disentanglement time being approximately half the conformational cycling period. This relationship is due to the similarity between the entanglements which occur during conformational cycling and the entanglements which occur when the electric field direction is changed.; The response of chains to a 180 degree change in field direction (field inversion) was investigated but, in contrast to the 120 degree case, no enhanced resolution was observed. The chains did not become entangled after field inversion in these simulations. These field inversion simulations were conducted in regular arrays of obstacles and it is believed that randomly oriented obstacles may be necessary to achieve enhanced resolution.
机译:用布朗动力学模拟研究了DNA的琼脂糖凝胶电泳。选择Langevin方程中的术语,即DNA链的运动方程,以尽可能逼真的表示DNA和琼脂糖。 DNA被建模为珠-弹簧链,而琼脂糖则被建模为规则排列的圆柱形障碍物的三维阵列。还完成了一些随机分布和定向障碍物的模拟。该模拟能够复制许多相关的实验现象。对于较短的链,仿真中的时间平均速度是链长度的强烈降低函数,但是对于较长的链,速度对链长度的这种依赖性消失了。对单个链的动态行为的研究表明,凝胶中链的运动以链在成束构象和延伸构象之间的循环为特征。此外,这种循环以特征周期发生,该特征周期取决于链的轮廓长度。研究了链对场方向突然120度变化的响应。预计在这些脉冲场模拟中会发生增强的分离。分辨率提高是由于场切换后发生纠缠。解缠结的特征在于解缠时间随链长线性变化。发现解缠时间和构象循环时间与解缠时间紧密相关,其大约为构象循环时间的一半。这种关系是由于在构象循环期间发生的缠结与在改变电场方向时发生的缠结之间的相似性。研究了链对场方向180度变化(场反转)的响应,但是与120度情况相反,没有观察到增强的分辨率。在这些模拟中,电场反转后,链没有纠缠在一起。这些场反转模拟是在规则的障碍物阵列中进行的,并且认为可能需要随机定向的障碍物才能获得更高的分辨率。

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