Dawn of a New RAMPage

Trends Pharmacol Sci. 2020 Apr;41(4):249-265. doi: 10.1016/j.tips.2020.01.009. Epub 2020 Feb 27.

Abstract

Receptor activity-modifying proteins (RAMPs) interact with G-protein-coupled receptors (GPCRs) to modify their functions, imparting significant implications upon their physiological and therapeutic potentials. Resurging interest in identifying RAMP-GPCR interactions has recently been fueled by coevolution studies and orthogonal technological screening platforms. These new studies reveal previously unrecognized RAMP-interacting GPCRs, many of which expand beyond Class B GPCRs. The consequences of these interactions on GPCR function and physiology lays the foundation for new molecular therapeutic targets, as evidenced by the recent success of erenumab. Here, we highlight recent papers that uncovered novel RAMP-GPCR interactions, human RAMP-GPCR disease-causing mutations, and RAMP-related human pathologies, paving the way for a new era of RAMP-targeted drug development.

Keywords: CGRP; G-protein-coupled receptor; adrenomedullin; coevolution; erenumab; receptor activity-modifying proteins (RAMPs).

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Antibodies, Monoclonal, Humanized / pharmacology
  • Calcitonin Gene-Related Peptide / metabolism
  • Calcitonin Gene-Related Peptide Receptor Antagonists / pharmacology
  • Humans
  • Molecular Targeted Therapy
  • Mutation
  • Receptor Activity-Modifying Proteins / genetics
  • Receptor Activity-Modifying Proteins / metabolism*
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, G-Protein-Coupled / metabolism*
  • Signal Transduction / drug effects

Substances

  • Antibodies, Monoclonal, Humanized
  • Calcitonin Gene-Related Peptide Receptor Antagonists
  • Receptor Activity-Modifying Proteins
  • Receptors, G-Protein-Coupled
  • erenumab
  • Calcitonin Gene-Related Peptide