Scientific Reports · 2019 · 28 citations · 15 references
MedicinePharmacologyExperimental PharmacologyMolecular PharmacologyPharmacodynamicsConcentration-effect RelationshipsModel BuildingReceptor BindingReceptor ModelingReceptor PharmacologyReceptor PhysiologyEquilibrium Dissociation ConstantFunctional Response ModelsLigand-receptor KineticsMuscarinic AgonistsMuscarinic Receptor SubtypesMuscarinic ReceptorsReceptor Kinetics ModelingReceptors
Abstract Proper determination of agonist efficacy is essential in the assessment of agonist selectivity and signalling bias. Agonist efficacy is a relative term that is dependent on the system in which it is measured, especially being dependent on receptor expression level. The operational model (OM) of functional receptor agonism is a useful means for the determination of agonist functional efficacy using the maximal response to agonist and ratio of agonist functional potency to its equilibrium dissociation constant (K A ) at the active state of the receptor. However, the functional efficacy parameter τ is inter-dependent on two other parameters of OM; agonist’s K A and the highest response that could be evoked in the system by any stimulus (E MAX ). Thus, fitting of OM to functional response data is a tricky process. In this work we analyse pitfalls of fitting OM to experimental data and propose a rigorous fitting procedure where K A and E MAX are derived from half-efficient concentration of agonist and apparent maximal responses obtained from a series of functional response curves. Subsequently, OM with fixed K A and E MAX is fitted to functional response data to obtain τ. The procedure was verified at M 2 and M 4 muscarinic receptors fused with the G 15 G-protein α-subunit. The procedure, however, is applicable to any receptor-effector system.
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Allosteric coupling from G protein to the agonist-binding pocket in GPCRs
Brian T. DeVree, Jacob P. Mahoney, Gisselle A. Vélez-Ruiz et al. · Nature · 2016 · 298 citations · Full text