Barbi M, Cocco S, Peyrard M, Ruffo S
Dipartimento di Fisica, Università degli Studi di Firenze, Largo E. Fermi, 2 - 50125 Firenze, Italy.
J Biol Phys. 1999 Jun;24(2-4):97-114. doi: 10.1023/A:1005139326775.
The real mechanisms of several biological processes involving DNA are not yet understood. We discuss here some aspects of the initiation of transcription, in particular the formation of the open complex and the activation mechanism associated to enhancer binding proteins. Transcription activation seems to be governed by underlying dynamical mechanisms related to several distortions of the double chain structure: a dynamical approach on a mesoscopic description level could then allow a deeper understanding of this complex process. Starting from the Peyrard Bishop (PB) model, that considers only the hydrogen bond stretching of each base pair, we describe here an extended DNA model, proposed in [1], that allows a rather good representation of the double helix geometry and of its structural features by the introduction of angular variables related to the twist angle. Using a generalized multiple scale expansion for the case of vectorial lattices derived elsewhere [2], we derive analytically small amplitude approximate solutions of the model which are movable and spatially localized: we present here the results of this calculation and show how the special shape of the solutions is in good agreement with what can be expected for coupled angular radial distortions in the real molecule.
涉及DNA的几个生物学过程的真正机制尚未被理解。我们在此讨论转录起始的一些方面,特别是开放复合物的形成以及与增强子结合蛋白相关的激活机制。转录激活似乎受与双链结构的几种扭曲相关的潜在动力学机制支配:那么在介观描述层面上的动力学方法可能会使我们对这个复杂过程有更深入的理解。从仅考虑每个碱基对氢键拉伸的佩拉尔 - 毕晓普(PB)模型出发,我们在此描述在[1]中提出的一个扩展DNA模型,该模型通过引入与扭转角相关的角变量,能够较好地表示双螺旋几何结构及其结构特征。对于在其他地方[2]推导的矢量晶格情况,使用广义多尺度展开,我们解析地推导了该模型的小振幅近似解,这些解是可移动的且在空间上是局部化的:我们在此展示此计算结果,并表明解的特殊形状与真实分子中耦合角径向扭曲所预期的情况非常吻合。