Literature DB >> 22579744

The structure of secretin family GPCR peptide ligands: implications for receptor pharmacology and drug development.

Harriet A Watkins1, Maggie Au, Debbie L Hay.   

Abstract

The secretin family G protein-coupled receptors, characterized by a large N-terminal extracellular domain and seven transmembrane helices, are drug targets in many diseases, including migraine, cardiovascular disease, diabetes, osteoporosis and inflammatory disorders. Their activating ligands are peptides with an average length of 30 amino acids. In this article we review the available structural data for these peptides and how this explains their activity. We emphasize how this information may be used to accelerate the development of new drugs against these receptors.
Copyright © 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 22579744     DOI: 10.1016/j.drudis.2012.05.005

Source DB:  PubMed          Journal:  Drug Discov Today        ISSN: 1359-6446            Impact factor:   7.851


  23 in total

Review 1.  Structural and functional insights into the juxtamembranous amino-terminal tail and extracellular loop regions of class B GPCRs.

Authors:  M Dong; C Koole; D Wootten; P M Sexton; L J Miller
Journal:  Br J Pharmacol       Date:  2014-03       Impact factor: 8.739

2.  Selective CGRP and adrenomedullin peptide binding by tethered RAMP-calcitonin receptor-like receptor extracellular domain fusion proteins.

Authors:  Heather E Moad; Augen A Pioszak
Journal:  Protein Sci       Date:  2013-10-19       Impact factor: 6.725

3.  Molecular basis of peptide activation of the GLP-1 receptor.

Authors:  Laurence J Miller
Journal:  Mol Metab       Date:  2013-03-06       Impact factor: 7.422

Review 4.  Structure of Class B GPCRs: new horizons for drug discovery.

Authors:  Andrea Bortolato; Andrew S Doré; Kaspar Hollenstein; Benjamin G Tehan; Jonathan S Mason; Fiona H Marshall
Journal:  Br J Pharmacol       Date:  2014-07       Impact factor: 8.739

5.  Use of Cysteine Trapping to Map Spatial Approximations between Residues Contributing to the Helix N-capping Motif of Secretin and Distinct Residues within Each of the Extracellular Loops of Its Receptor.

Authors:  Maoqing Dong; Polo C-H Lam; Andrew Orry; Patrick M Sexton; Arthur Christopoulos; Ruben Abagyan; Laurence J Miller
Journal:  J Biol Chem       Date:  2016-01-06       Impact factor: 5.157

Review 6.  Amylin structure-function relationships and receptor pharmacology: implications for amylin mimetic drug development.

Authors:  Rebekah L Bower; Debbie L Hay
Journal:  Br J Pharmacol       Date:  2016-05-18       Impact factor: 8.739

Review 7.  Outside-in signaling--a brief review of GPCR signaling with a focus on the Drosophila GPCR family.

Authors:  Caitlin D Hanlon; Deborah J Andrew
Journal:  J Cell Sci       Date:  2015-09-07       Impact factor: 5.285

Review 8.  Structure-activity relationships for α-calcitonin gene-related peptide.

Authors:  Harriet A Watkins; Dan L Rathbone; James Barwell; Debbie L Hay; David R Poyner
Journal:  Br J Pharmacol       Date:  2013-12       Impact factor: 8.739

9.  Structure-function analyses reveal a triple β-turn receptor-bound conformation of adrenomedullin 2/intermedin and enable peptide antagonist design.

Authors:  Amanda M Roehrkasse; Jason M Booe; Sang-Min Lee; Margaret L Warner; Augen A Pioszak
Journal:  J Biol Chem       Date:  2018-08-23       Impact factor: 5.157

Review 10.  Non-peptide agonists and positive allosteric modulators of glucagon-like peptide-1 receptors: Alternative approaches for treatment of Type 2 diabetes.

Authors:  Faisal Malik; Zhijun Li
Journal:  Br J Pharmacol       Date:  2021-04-19       Impact factor: 8.739

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