Modulation of glucagon receptor pharmacology by receptor activity-modifying protein-2 (RAMP2)

Cathryn Weston, Jing Lu, Naichang Li, Kerry Barkan, Gareth O. Richards, David J. Roberts, Timothy M. Skerry, David Poyner, Meenakshi Pardamwar, Christopher A. Reynolds, Simon J. Dowell, Gary B. Willars, Graham Ladds

Research output: Contribution to journalArticlepeer-review

53 Citations (Scopus)
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The glucagon and glucagon-like peptide-1 (GLP-1) receptors play important, opposing roles in regulating blood glucose levels. Consequently, these receptors have been identified as targets for novel diabetes treatments. However, drugs acting at the GLP-1 receptor, although having clinical efficacy, have been associated with severe adverse side-effects, and targeting of the glucagon receptor has yet to be successful. Here we use a combination of yeast reporter assays and mammalian systems to provide a more complete understanding of glucagon receptor signaling, considering the effect of multiple ligands, association with the receptor-interacting protein receptor activity-modifying protein-2 (RAMP2), and the role of individual G protein α-subunits. We demonstrate that RAMP2 alters both ligand selectivity and G protein preference of the glucagon receptor. Importantly, we also uncover novel cross-reactivity of therapeutically used GLP-1 receptor ligands at the glucagon receptor that is abolished by RAMP2 interaction. This study reveals the glucagon receptor as a previously unidentified target for GLP-1 receptor agonists and highlights a role for RAMP2 in regulating its pharmacology. Such previously unrecognized functions of RAMPs highlight the need to consider all receptor-interacting proteins in future drug development.

Original languageEnglish
Pages (from-to)23009-23022
Number of pages14
JournalJournal of Biological Chemistry
Issue number38
Early online date21 Jul 2015
Publication statusPublished - 18 Sept 2015
Externally publishedYes

Bibliographical note

Final version free via Creative Commons CC-BY license

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology


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