{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,18]],"date-time":"2026-08-18T01:28:49Z","timestamp":1787016529723,"version":"build-2736575974"},"reference-count":52,"publisher":"American Association for the Advancement of Science (AAAS)","issue":"900","license":[{"start":{"date-parts":[[2026,8,19]],"date-time":"2026-08-19T00:00:00Z","timestamp":1787097600000},"content-version":"vor","delay-in-days":365,"URL":"https:\/\/www.science.org\/content\/page\/science-licenses-journal-article-reuse"}],"content-domain":{"domain":["www.science.org"],"crossmark-restriction":true},"short-container-title":["Sci. Signal."],"published-print":{"date-parts":[[2025,8,19]]},"abstract":"<jats:p>\n                    Three amylin receptors (AMYRs) mediate the metabolic actions of the peptide hormone amylin and are drug targets for diabetes and obesity. AMY\n                    <jats:sub>1<\/jats:sub>\n                    R, AMY\n                    <jats:sub>2<\/jats:sub>\n                    R, and AMY\n                    <jats:sub>3<\/jats:sub>\n                    R are heterodimers consisting of the calcitonin receptor (CTR), a G protein\u2013coupled receptor, paired with a RAMP1, RAMP2, or RAMP3 accessory subunit, respectively, which increases amylin potency. Here, we found that the AMYRs had distinct basal subunit equilibria that were modulated by peptide agonists and determined the extent of cAMP signaling downstream of receptor activation. By developing a biochemical assay that resolves the AMYR heterodimers and free subunits, we found that the AMY\n                    <jats:sub>1<\/jats:sub>\n                    R and AMY\n                    <jats:sub>2<\/jats:sub>\n                    R subunit distributions favored free CTR and RAMPs and that rat amylin promoted association of the constituent subunits of AMY\n                    <jats:sub>1<\/jats:sub>\n                    R and AMY\n                    <jats:sub>2<\/jats:sub>\n                    R. The agonist \u03b1CGRP also induced AMY\n                    <jats:sub>1<\/jats:sub>\n                    R subunit association. A stronger interaction between the CTR and the RAMP3 transmembrane domains yielded a more stable AMY\n                    <jats:sub>3<\/jats:sub>\n                    R, and human and salmon calcitonin agonists promoted AMY\n                    <jats:sub>3<\/jats:sub>\n                    R dissociation. Similar changes in subunit association and dissociation were observed in live-cell membranes, and G protein coupling and cAMP signaling assays showed how these changes altered signaling. Our findings have implications for AMYR biology and drug development and reveal regulation of heteromeric GPCR signaling through subunit interaction dynamics.\n                  <\/jats:p>","DOI":"10.1126\/scisignal.adt8127","type":"journal-article","created":{"date-parts":[[2025,8,19]],"date-time":"2025-08-19T17:58:34Z","timestamp":1755626314000},"update-policy":"https:\/\/doi.org\/10.34133\/aaas_crossmark","source":"Crossref","is-referenced-by-count":6,"title":["Amylin receptor subunit interactions are modulated by agonists and determine signaling"],"prefix":"10.1126","volume":"18","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-3728-3767","authenticated-orcid":true,"given":"Sandra E.","family":"Gostynska","sequence":"first","affiliation":[{"name":"Department of Biochemistry and Physiology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-2001-5176","authenticated-orcid":true,"given":"Jordan A.","family":"Karim","sequence":"additional","affiliation":[{"name":"Department of Biochemistry and Physiology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Bailee E.","family":"Ford","sequence":"additional","affiliation":[{"name":"Department of Biochemistry and Physiology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0009-0009-5194-9586","authenticated-orcid":true,"given":"Peyton H.","family":"Gordon","sequence":"additional","affiliation":[{"name":"Department of Biochemistry and Physiology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-7357-393X","authenticated-orcid":true,"given":"Katie M.","family":"Babin","sequence":"additional","affiliation":[{"name":"Department of Biochemistry and Physiology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-0805-4049","authenticated-orcid":true,"given":"Asuka","family":"Inoue","sequence":"additional","affiliation":[{"name":"Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai 980-8578, Japan."},{"name":"Graduate School of Pharmaceutical Sciences, Kyoto University, Kyoto 606-8501, Japan."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-7550-0921","authenticated-orcid":true,"given":"Nevin A.","family":"Lambert","sequence":"additional","affiliation":[{"name":"Department of Pharmacology and 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