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Analytical Debye-Huckel model for electrostatic potentials around dissolved DNA.

机译:溶解DNA周围的静电势的解析Debye-Huckel模型。

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摘要

We present an analytical, Green-function-based model for the electric potential of DNA in solution, treating the surrounding solvent with the Debye-Huckel approximation. The partial charge of each atom is accounted for by modeling DNA as linear distributions of atoms on concentric cylindrical surfaces. The condensed ions of the solvent are treated with the Debye-Huckel approximation. The resultant leading term of the potential is that of a continuous shielded line charge, and the higher order terms account for the helical structure. Within several angstroms of the surface there is sufficient information in the electric potential to distinguish features and symmetries of DNA. Plots of the potential and equipotential surfaces, dominated by the phosphate charges, reflect the structural differences between the A, B, and Z conformations and, to a smaller extent, the difference between base sequences. As the distances from the helices increase, the magnitudes of the potentials decrease. However, the bases and sugars account for a larger fraction of the double helix potential with increasing distance. We have found that when the solvent is treated with the Debye-Huckel approximation, the potential decays more rapidly in every direction from the surface than it did in the concentric dielectric cylinder approximation.
机译:我们为溶液中DNA的电势提供了一个基于格林函数的分析模型,并通过Debye-Huckel近似法处理周围的溶剂。通过将DNA建模为同心圆柱表面上原子的线性分布,可以解释每个原子的部分电荷。用Debye-Huckel近似法处理溶剂的冷凝离子。电位的合成超前项是连续屏蔽线电荷的超前项,而高阶项则说明了螺旋结构。在表面的几埃内,电势中有足够的信息可以区分DNA的特征和对称性。由磷酸盐电荷控制的势能和等势面的图反映了A,B和Z构象之间的结构差异,并在较小程度上反映了碱基序列之间的差异。随着距螺旋距离的增加,电势的大小减小。然而,随着距离的增加,碱和糖占双螺旋势的较大部分。我们发现,当用Debye-Huckel近似法处理溶剂时,与同心介电圆柱体近似法相比,从表面到各个方向的电势衰减都更快。

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