Steric control of signaling bias in the immunometabolic receptor GPR84

Abstract

Abstract Biased signaling in G protein-coupled receptors offers therapeutic promise, yet rational design of biased ligands remains challenging due to limited mechanistic understanding. Here, we report a molecular basis for controlling signaling bias at the immunometabolic receptor GPR84. We identify three structurally-matched ligands (OX04529, OX04954, and OX04539) with varying steric profiles that exhibit comparable G i protein activation but markedly different β-arrestin recruitment capacities. A high-resolution cryo-EM structure of GPR84-G i in complex with OX04529, complemented by molecular dynamics simulations and targeted mutagenesis, reveals that steric interactions between ligand substituents and Leu336 6.52 and Phe187 5.47 indirectly disrupt a critical polar network involving Tyr332 6.48 , Asn104 3.36 and Asn362 7.45 essential for β-arrestin recruitment. Based on these insights, we develop a steric-dependent model that enables rational design of G protein-biased agonists with predictable β-arrestin recruitment profiles. This mechanistic framework provides the means to design biased agonists with customized signaling profiles at GPR84 and potentially other class A GPCRs.