The G-protein coupled receptors (GPCRs) play fundamental roles in the human biololgy and drug discovery. GPCRs function as signalling molecules that transduce extracellular signals into cells. The signalling transduction is generally triggered by interacting with ligands, including photons, ions, small organic compounds, peptides, proteins and lipids. In this review, we focus on interactions with diffusible ligands such as hormones and neurotransmitters. We discuss three aspects of the complexity of the GPCR-ligand interactions: functional selectivity of ligands, receptor subtype selectivity of ligands and orphan GPCRs.
机构:
Genome Center, University of California, 451 East Health Science Drive,Davis, CA 95616, USAGenome Center, University of California, 451 East Health Science Drive,Davis, CA 95616, USA
机构:
Rockefeller Univ, Lab Chem Biol & Signal Transduct, New York, NY 10065 USARockefeller Univ, Lab Chem Biol & Signal Transduct, New York, NY 10065 USA
Grunbeck, Amy
Sakmar, Thomas P.
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Rockefeller Univ, Lab Chem Biol & Signal Transduct, New York, NY 10065 USARockefeller Univ, Lab Chem Biol & Signal Transduct, New York, NY 10065 USA
机构:
Univ Claude Bernard Lyon 1, Univ Lyon, CNRS, Ctr RMN Tres Hauts Champs,ENS, 5 Rue Doua, F-69100 Villeurbanne, FranceUniv Claude Bernard Lyon 1, Univ Lyon, CNRS, Ctr RMN Tres Hauts Champs,ENS, 5 Rue Doua, F-69100 Villeurbanne, France
Raingeval, Claire
Krimm, Isabelle
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Univ Claude Bernard Lyon 1, Univ Lyon, CNRS, Ctr RMN Tres Hauts Champs,ENS, 5 Rue Doua, F-69100 Villeurbanne, FranceUniv Claude Bernard Lyon 1, Univ Lyon, CNRS, Ctr RMN Tres Hauts Champs,ENS, 5 Rue Doua, F-69100 Villeurbanne, France