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Comparison of all atom, continuum, and linear fitting empirical models for charge screening effect of aqueous medium surrounding

机译:比较所有原子,连续体和线性拟合经验模型对周围水介质的电荷屏蔽效果

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To investigate the role hydration plays in the electrostatic interactions of proteins, the time-averaged electrostatic potential of the B1 domain of protein G in an aqueous solution was calculated with full atomic molecular dynamics simulations that explicitly considers every atom (i.e., an all atom model). This all atom calculated potential was compared with the potential obtained from an electrostatic continuum model calculation. In both cases, the charge-screening effect was fairly well formulated with an effective relative dielectric constant which increased linearly with increasing charge-charge distance. This simulated linear dependence agrees with the experimentally determined linear relation proposed by Pickersgill. Cut-off approximations for Coulomb interactions failed to reproduce this linear relation. Correlation between the all atom model and the continuum models was found to be better than the respective correlation calculated for linear fitting to the two models. This confirms that the continuum model is better at treating the complicated shapes of protein conformations than the simple linear fitting empirical model. We have tried a sigmoid fitting empirical model in addition to the linear one. When weights of all data were treated equally, the sigmoid model, which requires two fitting parameters, fits results of both the all atom and the continuum models less accurately than the linear model which requires only one fitting parameter. When potential values are chosen as weighting factors, the fitting error of the sigmoid model became smaller, and the slope of both linear fitting curves became smaller. This suggests the screening effect on an aqueous medium within a short range, where potential values are relatively large, is smaller than that expected from the linear fitting curve whose slope is almost 4. To investigate the linear increase of the effective relative dielectric constant, the Poisson equation of a low-dielectric sphere in a high-dielectric medium was solved and charges distributed near the molecular surface were indicated as leading to the apparent linearity.
机译:为了研究水合作用在蛋白质静电相互作用中的作用,使用完全考虑了每个原子(即全原子模型)的完整原子分子动力学模拟,计算了水溶液中蛋白质G的B1域的时间平均静电势。 )。将所有原子计算的电势与从静电连续谱模型计算获得的电势进行比较。在这两种情况下,电荷屏蔽效应都用有效的相对介电常数制定得很好,该相对介电常数随电荷-电荷距离的增加而线性增加。这种模拟的线性相关性与Pickersgill提出的实验确定的线性关系一致。库仑相互作用的截断近似未能重现此线性关系。发现所有原子模型和连续体模型之间的相关性比为线性拟合两个模型而计算的相应相关性更好。这证实了连续体模型比简单的线性拟合经验模型在处理复杂的蛋白质构象形状方面更好。除了线性模型外,我们还尝试了S型拟合的经验模型。当所有数据的权重均等地对待时,需要两个拟合参数的S形模型与仅需要一个拟合参数的线性模型相比,对所有原子模型和连续谱模型的结果拟合的准确性都较低。当电势值被选择为加权因子,乙状结肠模型的拟合误差变小,并且两个线性拟合曲线的斜率变小。这表明对电位值相对较大的短距离水性介质的屏蔽作用小于斜率接近4的线性拟合曲线所预期的屏蔽作用。要研究有效相对介电常数的线性增加,解决了高介电介质中低介电球的泊松方程,表明分子表面附近分布的电荷导致表观线性。

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