Abstract
Molecular dynamics (MD) simulations were carried out to study the conformational rearrangement induced by deprotonation of the fluorescent chromophore in GFP, as well as the associated changes in the hydrogen‐bonding network. For both the structures with either a neutral or an anionic chromophore, it was found that the β‐barrel was stable and rigid, and the conformation of the chromophore was consistent with the available x‐ray structure. The conformational change in Thr203 due to deprotonation was also found to be consistent with the three‐state isomerization model. Although GFP is highly fluorescent, denatured‐GFP is nonfluorescent, indicating that the environment of the protein plays an important role in its fluorescence behavior. Our MD simulations, which explore the effect of the protein shell on the conformation of the chromophore, find the flexibility of the central chromophore to be significantly restricted due to the rigid nature of the protein shell. The hydrogen‐bonding between the chromophore and neighboring residues was also shown to contribute to the chromophore rigidity. In addition to the MD studies, quantum mechanics/molecular mechanics (QM/MM) ONIOM calculations were carried out to investigate the effect of the β‐barrel on the internal rotation in the chromophore. Along with providing quantitative values for torsional rotation barriers about the bridging bond in the chromophore, the ONIOM calculations also validate our MD force field parameters. © 2004 Wiley Periodicals, Inc. Biopolymers, 2004