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bioRxiv · 10.1101/2024.10.09.617487

Amylin receptor subunit interactions are modulated by agonists and determine signaling

Gostynska, S. E.·Karim, J. A.·Ford, B. E.·Gordon, P. H.·Babin, K. M.·Inoue, A.·Lambert, N. A.·Pioszak, A. A.
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Abstract

Three amylin receptors (AMYRs) mediate the metabolic actions of the peptide hormone amylin and are drug targets for diabetes and obesity. AMY1R, AMY2R, and AMY3R are heterodimers consisting of the G protein-coupled calcitonin receptor (CTR) paired with a RAMP1, -2, or -3 accessory subunit, respectively, which increases amylin potency. Little is known about AMYR subunit interactions and their role in signaling. Here, we show that the AMYRs have distinct basal subunit equilibriums that are modulated by peptide agonists and determine the cAMP signaling phenotype. Using a novel biochemical assay that resolves the AMYR heterodimers and free subunits, we found that the AMY1/2R subunit equilibriums favored free CTR and RAMP1/2, and rat amylin and CGRP agonists promoted subunit association. A stronger CTR-RAMP3 transmembrane domain interface yielded a more stable AMY3R, and human and salmon calcitonin agonists promoted AMY3R dissociation. Similar changes in subunit association-dissociation were observed in live cell membranes, and G protein coupling and cAMP signaling assays showed how these altered signaling. Our findings reveal regulation of heteromeric GPCR signaling through subunit interaction dynamics.

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Gostynska, S. E., Karim, J. A., Ford, B. E., Gordon, P. H., Babin, K. M., Inoue, A., Lambert, N. A., Pioszak, A. A.. 2024-10-09. Amylin receptor subunit interactions are modulated by agonists and determine signaling. https://doi.org/10.1101/2024.10.09.617487

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