<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Klein KR</submitter><funding>NIDDK NIH HHS</funding><funding>NHLBI NIH HHS</funding><pagination>65-71</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4911013</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>51(1)</volume><pubmed_abstract>Receptor activity modifying proteins (RAMPs) associate with G-protein-coupled receptors (GPCRs) at the plasma membrane and together bind a variety of peptide ligands, serving as a communication interface between the extracellular and intracellular environments. The collection of RAMP-interacting GPCRs continues to expand and now consists of GPCRs from families A, B and C, suggesting that RAMP activity is extremely prevalent. RAMP association with GPCRs can regulate GPCR function by altering ligand binding, receptor trafficking and desensitization, and downstream signaling pathways. Here, we elaborate on these RAMP-dependent mechanisms of GPCR regulation, which provide opportunities for pharmacological intervention.</pubmed_abstract><journal>Critical reviews in biochemistry and molecular biology</journal><pubmed_title>The expanding repertoire of receptor activity modifying protein (RAMP) function.</pubmed_title><pmcid>PMC4911013</pmcid><funding_grant_id>DK099156</funding_grant_id><funding_grant_id>R01 DK099156</funding_grant_id><funding_grant_id>F30 HL118932</funding_grant_id><pubmed_authors>Klein KR</pubmed_authors><pubmed_authors>Matson BC</pubmed_authors><pubmed_authors>Caron KM</pubmed_authors></additional><is_claimable>false</is_claimable><name>The expanding repertoire of receptor activity modifying protein (RAMP) function.</name><description>Receptor activity modifying proteins (RAMPs) associate with G-protein-coupled receptors (GPCRs) at the plasma membrane and together bind a variety of peptide ligands, serving as a communication interface between the extracellular and intracellular environments. The collection of RAMP-interacting GPCRs continues to expand and now consists of GPCRs from families A, B and C, suggesting that RAMP activity is extremely prevalent. RAMP association with GPCRs can regulate GPCR function by altering ligand binding, receptor trafficking and desensitization, and downstream signaling pathways. Here, we elaborate on these RAMP-dependent mechanisms of GPCR regulation, which provide opportunities for pharmacological intervention.</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Jan-Feb</publication><modification>2021-02-19T11:51:57Z</modification><creation>2019-03-27T02:16:14Z</creation></dates><accession>S-EPMC4911013</accession><cross_references><pubmed>26740457</pubmed><doi>10.3109/10409238.2015.1128875</doi></cross_references></HashMap>