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Agonist Binding and G Protein Coupling in Histamine H(2) Receptor: A Molecular Dynamics Study
The histamine H [Formula: see text] receptor (H(2)R) plays an important role in the regulation of gastric acid secretion. Therefore, it is a main drug target for the treatment of gastroesophageal reflux or peptic ulcer disease. However, there is as of yet no 3D-structural information available hampe...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7554837/ https://www.ncbi.nlm.nih.gov/pubmed/32932742 http://dx.doi.org/10.3390/ijms21186693 |
Sumario: | The histamine H [Formula: see text] receptor (H(2)R) plays an important role in the regulation of gastric acid secretion. Therefore, it is a main drug target for the treatment of gastroesophageal reflux or peptic ulcer disease. However, there is as of yet no 3D-structural information available hampering a mechanistic understanding of H(2)R. Therefore, we created a model of the histamine-H(2)R-G(s) complex based on the structure of the ternary complex of the [Formula: see text]-adrenoceptor and investigated the conformational stability of this active GPCR conformation. Since the physiologically relevant motions with respect to ligand binding and conformational changes of GPCRs can only partly be assessed on the timescale of conventional MD (cMD) simulations, we also applied metadynamics and Gaussian accelerated molecular dynamics (GaMD) simulations. A multiple walker metadynamics simulation in combination with cMD was applied for the determination of the histamine binding mode. The preferential binding pose detected is in good agreement with previous data from site directed mutagenesis and provides a basis for rational ligand design. Inspection of the H(2)R-G(s) interface reveals a network of polar interactions that may contribute to H(2)R coupling selectivity. The cMD and GaMD simulations demonstrate that the active conformation is retained on a [Formula: see text] s-timescale in the ternary histamine-H(2)R-G(s) complex and in a truncated complex that contains only G(s) helix [Formula: see text] 5 instead of the entire G protein. In contrast, histamine alone is unable to stabilize the active conformation, which is in line with previous studies of other GPCRs. |
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