Department of Chemical and Biological Engineering, Koc University, Istanbul, Turkey.
PLoS One. 2010 Oct 12;5(10):e13275. doi: 10.1371/journal.pone.0013275.
An optimization model is introduced in which proteins try to evade high energy regions of the folding landscape, and prefer low entropy loss routes during folding. We make use of the framework of optimal control whose convenient solution provides practical and useful insight into the sequence of events during folding. We assume that the native state is available. As the protein folds, it makes different set of contacts at different folding steps. The dynamic contact map is constructed from these contacts. The topology of the dynamic contact map changes during the course of folding and this information is utilized in the dynamic optimization model. The solution is obtained using the optimal control theory. We show that the optimal solution can be cast into the form of a Gaussian Network that governs the optimal folding dynamics. Simulation results on three examples (CI2, Sso7d and Villin) show that folding starts by the formation of local clusters. Non-local clusters generally require the formation of several local clusters. Non-local clusters form cooperatively and not sequentially. We also observe that the optimal controller prefers "zipping" or small loop closure steps during folding. The folding routes predicted by the proposed method bear strong resemblance to the results in the literature.
引入了一个优化模型,其中蛋白质试图逃避折叠景观的高能区域,并在折叠过程中优先选择低熵损失途径。我们利用最优控制的框架,其方便的解决方案为折叠过程中的事件序列提供了实用且有用的见解。我们假设天然状态是可用的。随着蛋白质的折叠,它在不同的折叠步骤中形成不同的接触。动态接触图是从这些接触中构建的。在折叠过程中,动态接触图的拓扑结构发生变化,并且该信息被利用于动态优化模型中。该解决方案是使用最优控制理论获得的。我们表明,最优解可以表示为控制最优折叠动力学的高斯网络。对三个示例(CI2、Sso7d 和 Villin)的模拟结果表明,折叠首先通过形成局部簇开始。非局部簇通常需要形成几个局部簇。非局部簇协同形成,而不是顺序形成。我们还观察到,最优控制器在折叠过程中更喜欢“拉链”或小环闭合步骤。所提出的方法预测的折叠路径与文献中的结果非常相似。