Adhesion G Protein–Coupled Receptors: From In Vitro Pharmacology to In Vivo Mechanisms
Author(s) -
Kelly R. Monk,
Jörg Hamann,
Tobias Langenhan,
Saskia Nijmeijer,
Torsten Schöneberg,
Ines Liebscher
Publication year - 2015
Publication title -
molecular pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.469
H-Index - 198
eISSN - 1521-0111
pISSN - 0026-895X
DOI - 10.1124/mol.115.098749
Subject(s) - receptor , signal transduction , computational biology , in vivo , g protein coupled receptor , microbiology and biotechnology , in vitro , biology , neuroscience , chemistry , biochemistry , genetics
The adhesion family of G protein-coupled receptors (aGPCRs) comprises 33 members in humans. aGPCRs are characterized by their enormous size and complex modular structures. While the physiologic importance of many aGPCRs has been clearly demonstrated in recent years, the underlying molecular functions have only recently begun to be elucidated. In this minireview, we present an overview of our current knowledge on aGPCR activation and signal transduction with a focus on the latest findings regarding the interplay between ligand binding, mechanical force, and the tethered agonistic Stachel sequence, as well as implications on translational approaches that may derive from understanding aGPCR pharmacology.
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