Revealing G-protein-coupled receptor oligomerization at the single-molecule level through a nanoscopic lens: methods, dynamics and biological function. (Q38618328)

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English	Revealing G-protein-coupled receptor oligomerization at the single-molecule level through a nanoscopic lens: methods, dynamics and biological function.	scientific article

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28 February 2020

Revealing G-protein-coupled receptor oligomerization at the single-molecule level through a nanoscopic lens: methods, dynamics and biological function (English)

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28 February 2020

G protein-coupled receptor

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Marco Scarselli

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28 February 2020

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Paolo Annibale

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28 February 2020

Peter J McCormick

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28 February 2020

Shivakumar Kolachalam

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28 February 2020

Stefano Aringhieri

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28 February 2020

Aleksandra Radenovic

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28 February 2020

Giovanni U Corsini

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28 February 2020

Roberto Maggio

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28 February 2020

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28 November 2015

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28 February 2020

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28 February 2020

283

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28 February 2020

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28 February 2020

1197-1217

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28 February 2020

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Time-resolved FRET between GPCR ligands reveals oligomers in native tissues.

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Old and new ways to calculate the affinity of agonists and antagonists interacting with G-protein-coupled monomeric and dimeric receptors: the receptor-dimer cooperativity index.

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Single-molecule imaging revealed dynamic GPCR dimerization

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Full characterization of GPCR monomer-dimer dynamic equilibrium by single molecule imaging

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Oligomer size of the serotonin 5-hydroxytryptamine 2C (5-HT2C) receptor revealed by fluorescence correlation spectroscopy with photon counting histogram analysis: evidence for homodimers without monomers or tetramers

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Fluorescence correlation spectroscopy analysis of serotonin, adrenergic, muscarinic, and dopamine receptor dimerization: the oligomer number puzzle

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Native serotonin 5-HT2C receptors are expressed as homodimers on the apical surface of choroid plexus epithelial cells

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Conformational biosensors reveal GPCR signalling from endosomes.

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Single molecule analysis of functionally asymmetric G protein-coupled receptor (GPCR) oligomers reveals diverse spatial and structural assemblies.

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Major ligand-induced rearrangement of the heptahelical domain interface in a GPCR dimer.

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Dual agonist occupancy of AT1-R-α2C-AR heterodimers results in atypical Gs-PKA signaling

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Plasma membrane diffusion of G protein-coupled receptor oligomers

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