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Rajarathnam, K.

Publications and source records attributed to Rajarathnam, K..

2 recordsLinked to original sources

CXCR1 and CXCR2 display receptor bias for shared chemokine agonists

G protein-coupled receptors (GPCRs) mediate diverse signaling outputs through their proximal transducers: G proteins, GRKs, and {beta}-arrestins. Although ligand bias at chemokine receptors (CKRs), where ligands for the same receptor display distinct signaling patterns, is well recognized, receptor bias, where the same agonist at different receptors yields distinct transducer engagement, remains poorly understood. We compared endogenous chemokine ligands (CXCL1, CXCL5, CXCL7, CXCL8) at the highly homologous CXCR1 and CXCR2 receptors using biosensor assays to measure Gi activation, {beta}-arrestin1/2 recruitment, GRK2/3/5/6 translocation, and receptor internalization. Our data reveal qualitatively different signaling patterns, most notably where CXCL1 acts as a G protein-biased partial agonist at CXCR1 but as a balanced full agonist at CXCR2. These signaling differences correlate with receptor internalization but not subcellular ERK activation patterns measured using compartment-specific biosensors. Collectively, our findings demonstrate receptor bias in CKR signaling, transducer activation, and compartmentalized kinase activation in translating chemokine identity into discrete functional outcomes. SIGNIFICANCE STATEMENTChemokine ligand bias, where different ligands for the same receptor display different signaling patterns, is now well appreciated. However, there are only few examples of receptor bias, where the same agonist generates distinct signaling profiles at different receptors. Here we used biosensors and compartmental ERK biosensors, to show that CXCL1, CXCL5, CXCL7, and CXCL8 differentially engage G proteins, {beta}-arrestins, and GRKs, at CXCR1 and CXCR2. This work provides mechanistic insight into CXCR1/CXCR2 signaling diversity.

biochemistry↗

Long-range coupled motions underlie ligand recognition by a chemokine receptor

Chemokines are unusual class-A GPCR agonists because of their large size ([~]10 kDa) and binding at two distinct receptor sites: N-terminal domain (Site-I, unique to chemokines) and a groove defined by extracellular loop/transmembrane helices (Site-II, shared with all small molecule class-A ligands). Whereas binding at Site-II triggers receptor activation, the role of Site-I is not known. Structures and sequence analysis reveal that the receptor N-terminal domains (N-domains) are flexible and contain intrinsic disorder. Using a hybrid NMR-MD approach, we characterized the role of Site-I interactions for the CXCL8-CXCR1 pair. NMR data indicate that the CXCR1 N-domain becomes structured on binding and that the binding interface is extensive with 30% of CXCL8 residues participating in this initial interaction. MD simulations indicate that CXCL8 bound at Site-I undergoes extensive reorganization on engaging Site-II with several residues initially engaged at Site-I also engaging Site-II. We conclude that structural plasticity of Site-I interactions plays an active role in driving ligand recognition by a chemokine receptor.

biophysics↗