Journal of the American Chemical Society · 2007 · 70 citations · 15 references
Life SciencesBiochemistryMolecular BiologyDrug DesignDrug DiscoveryStructural BiologyDrug-receptor InteractionsLigand BindingMolecular DynamicsProtein StructureProtein Structure ModelingReceptor ModelingAlpha HelicesEgressG Protein-coupled Receptor BindingG Protein-coupled Receptor ModelingG Protein-coupled Receptor Structure-function RelationshipsG-protein-coupled ReceptorsProtein-ligand Binding ModelingTransmembrane Helices
Rhodopsin serves as the prototype for studies of the G-protein coupled receptor (GPCR) proteins as it is the only GPCR protein with known crystal structures, and its structure has been used as the template to model a large number of GPCR proteins, including many used as drug targets. Understanding ligand entrance routes is important for designing drugs with improved efficacy. Here we simulated the egress of the retinal chromophore from the protein by applying the random acceleration molecular dynamics (RAMD) method. The interhelical clefts near the extracellular side were identified to be the predominant egress, while the movement of retinal deep into the cytoplasmic side was also observed. These results suggest possible routes for ligands to enter into the binding pockets of GPCR proteins. In addition, the RAMD simulation results revealed the high stability of the interactions between helix 3 and other helices.
15
Development and testing of a general amber force field
Junmei Wang, Romain M. Wolf, James W. Caldwell et al. · Journal of Computational Chemistry · 2004 · 19.6K citations
The Amber biomolecular simulation programs
David A. Case, Thomas E. Cheatham, Tom Darden et al. · Journal of Computational Chemistry · 2005 · 9.6K citations · Full text
Crystal Structure of Rhodopsin: A G Protein-Coupled Receptor
Krzysztof Palczewski, Takashi Kumasaka, Tetsuya Hori et al. · Science · 2000 · 5.6K citations