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使用隐藏约束对罕见事件进行采样。

Sampling of rare events using hidden restraints.

作者信息

Christen Markus, Kunz Anna-Pitschna E, van Gunsteren Wilfred F

机构信息

Laboratory of Physical Chemistry, Swiss Federal Institute of Technology Zürich, ETH, CH-8093 Zürich, Switzerland.

出版信息

J Phys Chem B. 2006 Apr 27;110(16):8488-98. doi: 10.1021/jp0604948.

Abstract

A method to enhance sampling of rare events is presented. It makes use of distance or dihedral-angle restraints to overcome an energy barrier separating two metastable states or to stabilize a transition state between the two metastable states. In order not to perturb these metastable end states themselves, a prefactor is introduced into the restraining energy function, which smoothly increases the weight of this function from zero to one at the transition state or on top of the separating energy barrier and then decreases the weight again to zero at the final state. The method is combined with multi-configurational thermodynamic integration and applied to two biomolecular systems, which were difficult to treat using standard thermodynamic integration. As first example the free energy difference of a cyclic alpha-aminoxy-hexapeptide-ion complex upon changing the ion from Cl- to Na+ was calculated. A large conformational rearrangement of the peptide was necessary to accommodate this change. Stabilizing the transition state by (hidden) restraints facilitates that. As a second example, the free energy difference between the 4C1 and the 1C4 conformation of beta-D-glucopyranoside was calculated. In unrestrained simulations the change from the 4C1 into the 1C4 conformation was never observed because of the high energy barrier separating the two states. Using (hidden) restraints, the transition from the 4C1 into the 1C4 state and back could be enforced without perturbing the end states. As comparison, for the same transitions the potential of mean force as obtained by using dihedral-angle constraints is provided.

摘要

本文提出了一种增强稀有事件采样的方法。该方法利用距离或二面角约束来克服分隔两个亚稳态的能量障碍,或稳定两个亚稳态之间的过渡态。为了不干扰这些亚稳态本身,在约束能量函数中引入了一个前置因子,该因子在过渡态或分隔能量障碍顶部将该函数的权重从零平滑增加到一,然后在终态再次将权重降至零。该方法与多构型热力学积分相结合,并应用于两个难以用标准热力学积分处理的生物分子系统。作为第一个例子,计算了环状α-氨基氧基-六肽-离子络合物在离子从Cl-变为Na+时的自由能差。肽需要进行大量的构象重排来适应这种变化。通过(隐藏)约束稳定过渡态有助于实现这一点。作为第二个例子,计算了β-D-吡喃葡萄糖苷的4C1和1C4构象之间的自由能差。在无约束模拟中,由于分隔这两个状态的高能垒,从未观察到从4C1构象到1C4构象的变化。使用(隐藏)约束,可以强制实现从4C1到1C4状态以及返回的转变,而不会干扰终态。作为比较,还提供了使用二面角约束获得的相同转变的平均力势。

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