Desruisseaux C, Slater G W, Kist T B
Department of Biology, University of Ottawa, Ontario, Canada.
Biophys J. 1998 Sep;75(3):1228-36. doi: 10.1016/S0006-3495(98)74042-1.
Recently, Griess and Serwer (1998. Biophys. J. 74:A71) showed that it was possible to use trapping electrophoresis and unbiased but asymmetrical electric field pulses to build a correlation ratchet that would allow the efficient separation of naked DNAs from identical DNAs that form a complex with a bulky object such as a protein. Here we present a theoretical investigation of this novel macromolecular separation process. We start by looking at the general features of this electrophoretic ratchet mechanism in the zero-frequency limit. We then examine the effects of finite frequencies on velocity and diffusion. Finally, we use the biased reptation model and computer simulations to understand the band-broadening processes. Our study establishes the main experimental regimes that can provide good resolution for specific applications.
最近,格里斯和塞尔韦尔(1998年,《生物物理杂志》第74卷:A71)表明,利用捕获电泳和无偏但不对称的电场脉冲构建相关棘轮,能够有效地从与蛋白质等大分子形成复合物的相同DNA中分离出裸DNA。在此,我们对这种新型大分子分离过程进行了理论研究。我们首先研究了零频率极限下这种电泳棘轮机制的一般特征。然后,我们考察了有限频率对速度和扩散的影响。最后,我们使用偏置蠕动模型和计算机模拟来理解谱带展宽过程。我们的研究确定了能够为特定应用提供良好分辨率的主要实验条件。