Protein Side Chain Modeling with Orientation-Dependent Atomic Force Fields Derived by Series Expansions
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We describe the development of new force fields for protein side chain modeling called optimized side chain atomic energy (OSCAR). The distance-dependent energy functions (OSCAR-d) and side-chain dihedral angle potential energy functions were represented as power and Fourier series, respectively. The resulting 802 adjustable parameters were optimized by discriminating the native side chain conformations from non-native conformations, using a training set of 12,000 side chains for each residue type. In the course of optimization, for every residue, its side chain was replaced by varying rotamers, whereas conformations for all other residues were kept as they appeared in the crystal structure. Then, the OSCAR-d were multiplied by an orientation-dependent function to yield OSCAR-o. A total of 1087 parameters of the orientation-dependent energy functions (OSCAR-o) were optimized by maximizing the energy gap between the native conformation and subrotamers calculated as low energy by OSCARd. When OSCAR-o with optimized parameters were used to model side chain conformations simultaneously for 218 recently released protein structures, the prediction accuracies were 88.8% for v1, 79.7% for v1 1 2, 1.24 A verall root mean square deviation (RMSD), and 0.62 A ࠒMSD for core residues, respectively, compared with the next-best performing side-chain modeling program which achieved 86.6% for v1, 75.7% for v1 1 2, 1.40 A verall RMSD, and 0.86 A ࠒMSD for core residues, respectively. The continuous energy functions obtained in this study are suitable for gradient-based optimization techniques for protein structure refinement.
Journal of Computational Chemistry
© 2011 Wiley Periodicals, Inc.. This is the accepted version of the following article: Protein Side Chain Modeling with Orientation-DependentAtomic Force Fields Derived by Series Expansions, Journal of Computational Chemistry, Vol. 32(8), 2011, pp. 1680-1686, which has been published in final form at dx.doi.org/10.1002/jcc.21747.