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Drug Discov Today. 2009 Apr;14(7-8):413-9. doi: 10.1016/j.drudis.2008.12.009. Epub 2009 Jan 16.

Modulating receptor function through RAMPs: can they represent drug targets in themselves?

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  • 1Drug Discovery Biology Laboratory, Monash Institute of Pharmaceutical Sciences and Department of Pharmacology, Monash University, Victoria 3800, Australia.

Abstract

G protein-coupled receptors (GPCRs) are successfully exploited as drug targets. As our understanding of how distinct GPCR subtypes can be generated expands, so do possibilities for therapeutic intervention via these receptors. Receptor activity-modifying proteins (RAMPs) are excellent examples of proteins that enhance diversity in GPCR function. They facilitate the creation of binding pockets, controlling the pharmacology of some GPCRs. Moreover, they have the ability to regulate cell-surface trafficking, internalisation and signalling of GPCRs, creating novel opportunities for drug discovery. RAMPs could be directly targeted by drugs, or advantage could be taken of unique RAMP/GPCR interfaces for generating highly selective ligands.

PMID:
19150656
[PubMed - indexed for MEDLINE]
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