Bivalent ligands promote endosomal trafficking of the dopamine D3 receptor-neurotensin receptor 1 heterodimer

Budzinski et al use bivalent ligands, BRET assays and radioligand competition to demonstrate a specific interaction between two receptors associated with neuropsychiatric diseases and addiction, dopamine D3 (D3R) and neurotensin receptor 1. They show that the bivalent ligands promote endosomal traff...

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Autores principales: Julian Budzinski, Simone Maschauer, Hiroyuki Kobayashi, Pierre Couvineau, Hannah Vogt, Peter Gmeiner, Anna Roggenhofer, Olaf Prante, Michel Bouvier, Dorothee Weikert
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Lenguaje:EN
Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/c19eeb6e87c441afa774ebbb7ead711b
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spelling oai:doaj.org-article:c19eeb6e87c441afa774ebbb7ead711b2021-12-02T17:19:12ZBivalent ligands promote endosomal trafficking of the dopamine D3 receptor-neurotensin receptor 1 heterodimer10.1038/s42003-021-02574-42399-3642https://doaj.org/article/c19eeb6e87c441afa774ebbb7ead711b2021-09-01T00:00:00Zhttps://doi.org/10.1038/s42003-021-02574-4https://doaj.org/toc/2399-3642Budzinski et al use bivalent ligands, BRET assays and radioligand competition to demonstrate a specific interaction between two receptors associated with neuropsychiatric diseases and addiction, dopamine D3 (D3R) and neurotensin receptor 1. They show that the bivalent ligands promote endosomal trafficking of D3R, suggesting a potential role for dimerization in vivo.Julian BudzinskiSimone MaschauerHiroyuki KobayashiPierre CouvineauHannah VogtPeter GmeinerAnna RoggenhoferOlaf PranteMichel BouvierDorothee WeikertNature PortfolioarticleBiology (General)QH301-705.5ENCommunications Biology, Vol 4, Iss 1, Pp 1-13 (2021)
institution DOAJ
collection DOAJ
language EN
topic Biology (General)
QH301-705.5
spellingShingle Biology (General)
QH301-705.5
Julian Budzinski
Simone Maschauer
Hiroyuki Kobayashi
Pierre Couvineau
Hannah Vogt
Peter Gmeiner
Anna Roggenhofer
Olaf Prante
Michel Bouvier
Dorothee Weikert
Bivalent ligands promote endosomal trafficking of the dopamine D3 receptor-neurotensin receptor 1 heterodimer
description Budzinski et al use bivalent ligands, BRET assays and radioligand competition to demonstrate a specific interaction between two receptors associated with neuropsychiatric diseases and addiction, dopamine D3 (D3R) and neurotensin receptor 1. They show that the bivalent ligands promote endosomal trafficking of D3R, suggesting a potential role for dimerization in vivo.
format article
author Julian Budzinski
Simone Maschauer
Hiroyuki Kobayashi
Pierre Couvineau
Hannah Vogt
Peter Gmeiner
Anna Roggenhofer
Olaf Prante
Michel Bouvier
Dorothee Weikert
author_facet Julian Budzinski
Simone Maschauer
Hiroyuki Kobayashi
Pierre Couvineau
Hannah Vogt
Peter Gmeiner
Anna Roggenhofer
Olaf Prante
Michel Bouvier
Dorothee Weikert
author_sort Julian Budzinski
title Bivalent ligands promote endosomal trafficking of the dopamine D3 receptor-neurotensin receptor 1 heterodimer
title_short Bivalent ligands promote endosomal trafficking of the dopamine D3 receptor-neurotensin receptor 1 heterodimer
title_full Bivalent ligands promote endosomal trafficking of the dopamine D3 receptor-neurotensin receptor 1 heterodimer
title_fullStr Bivalent ligands promote endosomal trafficking of the dopamine D3 receptor-neurotensin receptor 1 heterodimer
title_full_unstemmed Bivalent ligands promote endosomal trafficking of the dopamine D3 receptor-neurotensin receptor 1 heterodimer
title_sort bivalent ligands promote endosomal trafficking of the dopamine d3 receptor-neurotensin receptor 1 heterodimer
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/c19eeb6e87c441afa774ebbb7ead711b
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