Implicit solvent models for flexible protein-protein docking by molecular dynamics simulation.

Ting Wang; Rebecca C Wade

doi:10.1002/prot.10248

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Implicit solvent models for flexible protein-protein docking by molecular dynamics simulation.

Ting Wang·Rebecca C Wade

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Abstract

The suitability of three implicit solvent models for flexible protein-protein docking by procedures using molecular dynamics simulation is investigated. The three models are (i) the generalized Born (GB) model implemented in the program AMBER6.0; (ii) a distance-dependent dielectric (DDD) model; and (iii) a surface area-dependent model that we have parameterized and call the NPSA model. This is a distance-dependent dielectric model modified by neutralizing the ionizable side-chains and adding a surface area-dependent solvation term. These solvent models were first tested in molecular dynamics simulations at 300 K of the native structures of barnase, barstar, segment B1 of protein G, and three WW domains. These protein structures display a range of secondary structure contents and stabilities. Then, to investigate the performance of the implicit solvent models in protein docking, molecular dynamics simulations of barnase/barstar complexation, as well as PIN1 WW domain/peptide complexation, were conducted, starting from separated unbound structures. The simulations show that the NPSA model has significant advantages over the DDD and GB models in maintaining the native structures of the proteins and providing more accurate docked complexes.

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Bacterial Proteins Computational Biology Computer Simulation Enzyme Inhibitors Kinetics Macromolecular Substances Models, Molecular NIMA-Interacting Peptidylprolyl Isomerase Peptidylprolyl Isomerase Phosphopeptides Protein Binding Protein Structure, Secondary Protein Structure, Tertiary Proteins Ribonucleases Solvents Journal Article Research Support, Non-U.S. Gov't

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Ting Wang, Rebecca C Wade. 2003-01-01. Implicit solvent models for flexible protein-protein docking by molecular dynamics simulation.. https://doi.org/10.1002/prot.10248

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