Time-resolved FRET between GPCR ligands reveals oligomers in native tissues
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Open Access
- 11 July 2010
- journal article
- research article
- Published by Springer Science and Business Media LLC in Nature Chemical Biology
- Vol. 6 (8), 587-594
- https://doi.org/10.1038/nchembio.396
Abstract
No abstract availableKeywords
This publication has 50 references indexed in Scilit:
- Hetero-oligomerization of CCR2, CCR5, and CXCR4 and the Protean Effects of “Selective” AntagonistsJournal of Biological Chemistry, 2009
- Allosteric communication between protomers of dopamine class A GPCR dimers modulates activationNature Chemical Biology, 2009
- Crosstalk between GABAB and mGlu1a receptors reveals new insight into GPCR signal integrationThe EMBO Journal, 2009
- Building a new conceptual framework for receptor heteromersNature Chemical Biology, 2009
- Dopamine D2 receptors form higher order oligomers at physiological expression levelsThe EMBO Journal, 2008
- Cell-surface protein-protein interaction analysis with time-resolved FRET and snap-tag technologies: application to GPCR oligomerizationNature Methods, 2008
- Asymmetric conformational changes in a GPCR dimer controlled by G-proteinsThe EMBO Journal, 2006
- Dual Inhibition of β-Adrenergic and Angiotensin II Receptors by a Single AntagonistCirculation, 2003
- Fluorescent Pseudo-Peptide Linear Vasopressin Antagonists: Design, Synthesis, and Applications,Journal of Medicinal Chemistry, 1999
- Two aromatic residues regulate the response of the human oxytocin receptor to the partial agonist arginine vasopressinFEBS Letters, 1996