Heterodimers and family-B GPCRs: RAMPs, CGRP and adrenomedullin

A. C. Conner, J. Simms, D. L. Hay, K. Mahmoud, S. G. Howitt, M. Wheatley, D. R. Poyner

Research output: Contribution to journalConference article

38 Citations (Scopus)

Abstract

RAMPs (receptor activity-modifying proteins) are single-pass transmembrane proteins that associate with certain family-B GPCRs (G-protein-coupled receptors). Specifically for the CT (calcitonin) receptor-like receptor and the CT receptor, this results in profound changes in ligand binding and receptor pharmacology, allowing the generation of six distinct receptors with preferences for CGRP (CT gene-related peptide), adrenomedullin, amylin and CT. There are three RAMPs: RAMP1-RAMP3. The N-terminus appears to be the main determinant of receptor pharmacology, whereas the transmembrane domain contributes to association of the RAMP with the GPCR. The N-terminus of all members of the RAMP family probably contains two disulphide bondi; a potential third disulphide is found in RAMP1 and RAMP3. The N-terminus appears to be in close proximity to the ligand and plays a key role in its binding, either directly or indirectly. BIBN4096BS, a CGRP antagonist, targets RAMP1 and this gives the compound very high selectivity for the human CGRP1 receptor.

Original languageEnglish
Pages (from-to)843-846
Number of pages4
JournalBiochemical Society Transactions
Volume32
Issue number5
Early online date26 Oct 2004
DOIs
Publication statusPublished - Nov 2004
Externally publishedYes

Keywords

  • Adrenomedullin
  • Calcitonin gene-related peptide (CGRP)
  • Calcitonin receptor-like receptor
  • RAMP2
  • RAMP3
  • Receptor activity-modifying protein 1 (RAMP1)

ASJC Scopus subject areas

  • Biochemistry

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