Science Advances · 2020 · 97 citations · 33 references
PharmacyMedicinal ChemistryPharmacologyDrug DesignMolecular PharmacologyStructural BiologyAntibody StructureLigand BindingProtein StructureProtein-ligand BindingReceptor ModelingReceptor-ligand InteractionsAgonist AntibodiesAntibodiesCocrystal FormationExtracellular DomainsG Protein-coupled Receptor BindingG-protein-coupled ReceptorsReceptor-ligand Structural BiologyStructure-guided Lead Discovery
Developing antibody agonists targeting the human apelin receptor (APJ) is a promising therapeutic approach for the treatment of chronic heart failure. Here, we report the structure-guided discovery of a single-domain antibody (sdAb) agonist JN241-9, based on the cocrystal structure of APJ with an sdAb antagonist JN241, the first cocrystal structure of a class A G protein-coupled receptor (GPCR) with a functional antibody. As revealed by the structure, JN241 binds to the extracellular side of APJ, makes critical contacts with the second extracellular loop, and inserts the CDR3 into the ligand-binding pocket. We converted JN241 into a full agonist JN241-9 by inserting a tyrosine into the CDR3. Modeling and molecular dynamics simulation shed light on JN241-9-stimulated receptor activation, providing structural insights for finding agonistic antibodies against class A GPCRs.
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Structure of a β1-adrenergic G-protein-coupled receptor
Tony Warne, María J. Serrano‐Vega, Jillian G. Baker et al. · Nature · 2008 · 1.3K citations · Full text