Improvement of the Treatment of Loop Structures in the UNRES Force Field by Inclusion of Coupling between Backbone- and Side-Chain-Local Conformational States

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• 作者：Pawe艂 Krupa ; Adam K. Sieradzan ; S. Rackovsky ; Maciej Baranowski ; Stanis艂aw O艂dziej ; Harold A. Scheraga ; Adam Liwo ; Cezary Czaplewski
• 刊名：Journal of Chemical Theory and Computation
• 出版年：2013
• 出版时间：October 8, 2013
• 年：2013
• 卷：9
• 期：10
• 页码：4620-4632
• 全文大小：824K
• 年卷期：v.9,no.10(October 8, 2013)
• ISSN：1549-9626

文摘

The UNited RESidue (UNRES) coarse-grained model of polypeptide chains, developed in our laboratory, enables us to carry out millisecond-scale molecular-dynamics simulations of large proteins effectively. It performs well in ab initio predictions of protein structure, as demonstrated in the last Community Wide Experiment on the Critical Assessment of Techniques for Protein Structure Prediction (CASP10). However, the resolution of the simulated structure is too coarse, especially in loop regions, which results from insufficient specificity of the model of local interactions. To improve the representation of local interactions, in this work, we introduced new side-chain-backbone correlation potentials, derived from a statistical analysis of loop regions of 4585 proteins. To obtain sufficient statistics, we reduced the set of amino-acid-residue types to five groups, derived in our earlier work on structurally optimized reduced alphabets [Solis, A. D.; Rackovsky, S. Proteins: Struct., Func., Bioinf., 2000, 38, 149鈥?64], based on a statistical analysis of the properties of amino-acid structures. The new correlation potentials are expressed as one-dimensional Fourier series in the virtual-bond-dihedral angles involving side-chain centroids. The weight of these new terms was determined by a trial-and-error method, in which Multiplexed Replica Exchange Molecular Dynamics (MREMD) simulations were run on selected test proteins. The best average root-mean-square deviations (RMSDs) of the calculated structures from the experimental structures below the folding-transition temperatures were obtained with the weight of the new side-chain-backbone correlation potentials equal to 0.57. The resulting conformational ensembles were analyzed in detail by using the Weighted Histogram Analysis Method (WHAM) and Ward鈥檚 minimum-variance clustering. This analysis showed that the RMSDs from the experimental structures dropped by 0.5 脜 on average, compared to simulations without the new terms, and the deviation of individual residues in the loop region of the computed structures from their counterparts in the experimental structures (after optimum superposition of the calculated and experimental structure) decreased by up to 8 脜. Consequently, the new terms improve the representation of local structure.