Literature DB >> 29058771

Bioluminescence Resonance Energy Transfer Assay to Characterize Gi-Like G Protein Subtype-Dependent Functional Selectivity.

Hideaki Yano1, Marta Sánchez-Soto1, Sergi Ferré1.   

Abstract

G protein-coupled receptors (GPCRs) comprise the single most targeted protein class in pharmacology. G protein signaling transduces extracellular stimuli such as neurotransmitters into cellular responses. Although preference for a specific GPCR among different G protein families (e.g., Gs-, Gi-, or Gq-like proteins) is often well studied, preference for a specific G protein subtype (e.g., Gi1, Gi2, Gi3, Go1, and Go2) has received little attention. Due to tissue expression differences and potentially exploitable functional differences, G protein subtype-dependent functional selectivity is an attractive framework to expand GPCR drug development. Herein we present a bioluminescence resonance energy transfer (BRET)-based method to characterize functional selectivity among Gi-like protein subtypes. © 2017 by John Wiley & Sons, Inc.
Copyright © 2017 John Wiley & Sons, Inc.

Entities:  

Keywords:  BRET; G protein subtype; GPCR; catecholamine; functional selectivity

Mesh:

Substances:

Year:  2017        PMID: 29058771      PMCID: PMC5657550          DOI: 10.1002/cpns.38

Source DB:  PubMed          Journal:  Curr Protoc Neurosci        ISSN: 1934-8576


  17 in total

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Review 3.  Resonance energy transfer approaches in molecular pharmacology and beyond.

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Review 4.  Modulation of ion-channel function by G-protein-coupled receptors.

Authors:  B Hille
Journal:  Trends Neurosci       Date:  1994-12       Impact factor: 13.837

5.  Selective inhibition of adenylyl cyclase type V by the dopamine D3 receptor.

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Review 6.  Mammalian G proteins and their cell type specific functions.

Authors:  Nina Wettschureck; Stefan Offermanns
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Review 7.  The physiology, signaling, and pharmacology of dopamine receptors.

Authors:  Jean-Martin Beaulieu; Raul R Gainetdinov
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8.  Novel Bivalent Ligands Based on the Sumanirole Pharmacophore Reveal Dopamine D2 Receptor (D2R) Biased Agonism.

Authors:  Alessandro Bonifazi; Hideaki Yano; Michael P Ellenberger; Ludovic Muller; Vivek Kumar; Mu-Fa Zou; Ning Sheng Cai; Adrian M Guerrero; Amina S Woods; Lei Shi; Amy Hauck Newman
Journal:  J Med Chem       Date:  2017-03-16       Impact factor: 7.446

9.  Functionally selective dopamine D2/D3 receptor agonists comprising an enyne moiety.

Authors:  Christine Hiller; Ralf C Kling; Frank W Heinemann; Karsten Meyer; Harald Hübner; Peter Gmeiner
Journal:  J Med Chem       Date:  2013-06-17       Impact factor: 7.446

10.  Evidence for Noncanonical Neurotransmitter Activation: Norepinephrine as a Dopamine D2-Like Receptor Agonist.

Authors:  Marta Sánchez-Soto; Alessandro Bonifazi; Ning Sheng Cai; Michael P Ellenberger; Amy Hauck Newman; Sergi Ferré; Hideaki Yano
Journal:  Mol Pharmacol       Date:  2016-02-03       Impact factor: 4.436

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