Kulić Igor M, Mohrbach Hervé, Lobaskin Vladimir, Thaokar Rochish, Schiessel Helmut
Max-Planck-Institute for Polymer Research, Theory Group, PO Box 3148, D 55021 Mainz, Germany.
Phys Rev E Stat Nonlin Soft Matter Phys. 2005 Oct;72(4 Pt 1):041905. doi: 10.1103/PhysRevE.72.041905. Epub 2005 Oct 6.
We derive the single molecule equation of state (force-extension relation) for DNA molecules bearing sliding loops and deflection defects. Analytical results are obtained in the large force limit by employing an analogy with instantons in quantum mechanical tunneling problems. The results reveal a remarkable feature of sliding loops--an apparent strong reduction of the persistence length. We generalize these results to several other experimentally interesting situations ranging from rigid DNA-protein loops to the problem of anchoring deflections in atomic force microscopy stretching of semiflexible polymers. Expressions relating the force-extension measurements to the underlying loop or boundary deflection geometry are provided and applied to the case of the gal repressor dimer protein. The theoretical predictions are complemented and quantitatively confirmed by molecular dynamics simulations.
我们推导了带有滑动环和偏转缺陷的DNA分子的单分子状态方程(力-伸长关系)。通过与量子力学隧穿问题中的瞬子进行类比,在大力极限下获得了分析结果。结果揭示了滑动环的一个显著特征——持久长度明显大幅降低。我们将这些结果推广到其他几个实验上有趣的情况,从刚性DNA-蛋白质环到半柔性聚合物原子力显微镜拉伸中锚定偏转的问题。提供了将力-伸长测量与潜在的环或边界偏转几何形状相关联的表达式,并应用于半乳糖阻遏物二聚体蛋白的情况。理论预测通过分子动力学模拟得到补充和定量证实。