| Title: | Long-timescale molecular-dynamics simulations of the major urinary protein provide atomistic interpretations of the unusual thermodynamics of ligand binding |
| Address: | "School of Pharmacy and Centre for Biomolecular Sciences, University of Nottingham, Nottingham, United Kingdom" |
| DOI: | 10.1016/j.bpj.2010.03.055 |
| ISSN/ISBN: | 1542-0086 (Electronic) 0006-3495 (Print) 0006-3495 (Linking) |
| Abstract: | "The mouse major urinary protein (MUP) has proved to be an intriguing test bed for detailed studies on protein-ligand recognition. NMR, calorimetric, and modeling investigations have revealed that the thermodynamics of ligand binding involve a complex interplay between competing enthalpic and entropic terms. We performed six independent, 1.2 micros molecular-dynamics simulations on MUP--three replicates on the apo-protein, and three on the complex with the pheromone isobutylmethoxypyrazine. Our findings provide the most comprehensive picture to date of the structure and dynamics of MUP, and how they are modulated by ligand binding. The mechanical pathways by which amino acid side chains can transmit information regarding ligand binding to surface loops and either increase or decrease their flexibility (entropy-entropy compensation) are identified. Dewetting of the highly hydrophobic binding cavity is confirmed, and the results reveal an aspect of ligand binding that was not observed in earlier, shorter simulations: bound ligand retains extensive rotational freedom. Both of these features have significant implications for interpretations of the entropic component of binding. More generally, these simulations test the ability of current molecular simulation methods to produce a reliable and reproducible picture of protein dynamics on the microsecond timescale" |
| Keywords: | Animals Binding Sites *Entropy Ligands Mice *Molecular Dynamics Simulation Protein Binding Protein Conformation Protein Stability Proteins/*chemistry/*metabolism Pyrazines/metabolism Reproducibility of Results Time Factors; |
| Notes: | "MedlineRoy, Julie Laughton, Charles A eng BBF0114071/Biotechnology and Biological Sciences Research Council/United Kingdom Research Support, Non-U.S. Gov't 2010/07/27 Biophys J. 2010 Jul 7; 99(1):218-26. doi: 10.1016/j.bpj.2010.03.055" |
