Biased activation of the vasopressin V2 receptor probed by NMR, paramagnetic ligands, and molecular dynamics simulations

Gaibelet, G.; Fouillen, A.; Stephanie, R.; Orcel, H.; Mendre, C.; Kanso, A.; Lanotte, R.; Nguyen, J.; Dimon, J.; Urbach, S.; Sounier, R.; Granier, S.; Bonnet, D.; Cong, X.; Mouillac, B.; Demene, H.

doi:10.1101/2023.06.06.543947

bioRxiv · 10.1101/2023.06.06.543947

Biased activation of the vasopressin V2 receptor probed by NMR, paramagnetic ligands, and molecular dynamics simulations

Gaibelet, G.·Fouillen, A.·Stephanie, R.·Orcel, H.·Mendre, C.·Kanso, A.·Lanotte, R.·Nguyen, J.·Dimon, J.·Urbach, S.·Sounier, R.·Granier, S.·Bonnet, D.·Cong, X.·Mouillac, B.·Demene, H.

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Abstract

G protein-coupled receptors (GPCRs) control critical intercellular communications by responding to extracellular stimuli and undertaking conformational changes to convey signals to intracellular effectors. We combined NMR, molecular pharmacology, and molecular dynamics (MD) simulations to study the conformational diversity of the vasopressin V2 GPCR subtype (V2R) bound to different types of ligands: the antagonist tolvaptan, the endogenous unbiased agonist arginine-vasopressin, and MCF14, a Gs-protein biased agonist. We developed a double-labeling NMR scheme to study the conformational dynamics: V2R was subjected to lysine 13CH3 methylation, whereas the agonists were tagged with a paramagnetic probe. Paramagnetic relaxation enhancements were used to validate the ligand binding poses in the MD simulations. We found that the bias for the Gs protein over the {beta}-arrestin pathway involves interactions between the conserved NPxxY motif in the transmembrane helix (TM) 7 and a central hydrophobic patch in TM3, which constrains TM7 and likely inhibits {beta}-arrestin signaling. A similar mechanism was observed for the pathogenic mutation, I1303.43N, which constitutively activates the Gs protein without concomitant {beta}-arrestin recruitment. This mechanism resembles to opioid receptors findings indicating common patterns in class A GPCRs.

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Gaibelet, G., Fouillen, A., Stephanie, R., Orcel, H., Mendre, C., Kanso, A., Lanotte, R., Nguyen, J., Dimon, J., Urbach, S., Sounier, R., Granier, S., Bonnet, D., Cong, X., Mouillac, B., Demene, H.. 2023-06-07. Biased activation of the vasopressin V2 receptor probed by NMR, paramagnetic ligands, and molecular dynamics simulations. https://doi.org/10.1101/2023.06.06.543947

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