Influence of water-protein hydrogen bonding on the stability of Trp-cage miniprotein. A comparison between the TIP3P and TIP4P-Ew water models

• Published in: Physical chemistry chemical physics : PCCP 2011-11, Vol.13 (44), p.1984-19847
• Main Authors: Paschek, Dietmar, Day, Ryan, García, Angel E
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Chemistry; Exact sciences and technology; General and physical chemistry; Hydrogen Bonding; Molecular Dynamics Simulation; Molecular Sequence Data; Peptides - chemistry; Protein Folding; Protein Structure, Secondary; Protein Unfolding; Thermodynamics; Transition Temperature; Water - chemistry
• ISSN: 1463-9076; 1463-9084
• DOI: 10.1039/c1cp22110h

We report extensive replica exchange molecular dynamics (REMD) simulations on the folding/unfolding equilibrium of Trp-cage miniprotein using the Amber ff99SB all atom forcefield and TIP3P and TIP4P-Ew explicit water solvent models. REMD simulation-lengths in the 500 ns to the microsecond regime per replica are required to adequately sample the folding/unfolding equilibrium. We observe that this equilibrium is significantly affected by the choice of the water model. Compared with experimental data, simulations using the TIP3P solvent describe the stability of the Trp-cage quite realistically, providing a melting point which is just a few Kelvins above the experimental transition temperature of 317 K. The TIP4P-Ew model shifts the equilibrium towards the unfolded state and lowers the free energy of unfolding by about 3 kJ mol −1 at 280 K, demonstrating the need to fine-tune the protein-forcefield depending on the chosen water model. We report evidence that the main difference between the two water models is mostly due to the different solvation of polar groups of the peptide. The unfolded state of the Trp-cage is stabilized by an increasing number of hydrogen bonds, destabilizing the α-helical part of the molecule and opening the R-D salt bridge. By reweighting the strength of solvent-peptide hydrogen bonds by adding a hydrogen bond square well potential, we can fully recover the effect of the different water models and estimate the shift in population as due to a difference in hydrogen bond-strength of about 0.4 kJ mol −1 per hydrogen bond. Varying the strength of water-peptide hydrogen bonds significantly shifts the equilibrium between folded and unfolded states of the Trp-cage miniprotein.