Fluorescent Tools for the Imaging of Dopamine D2‐Like Receptors**

Author:

Nagl Martin1,Mönnich Denise1,Rosier Niklas1ORCID,Schihada Hannes2ORCID,Sirbu Alexei3ORCID,Konar Nergis3,Reyes‐Resina Irene45ORCID,Navarro Gemma45ORCID,Franco Rafael46ORCID,Kolb Peter2,Annibale Paolo37,Pockes Steffen18ORCID

Affiliation:

1. Institute of Pharmacy University of Regensburg Universitätsstraße 31 D-93053 Regensburg Germany

2. Department of Pharmaceutical Chemistry University of Marburg Marbacher Weg 6 35037 Marburg Germany

3. Max Delbrück Center for Molecular Medicine Berlin 13125 Germany

4. CiberNed Network Center for Neurodegenerative diseases National Spanish Health Institute Carlos III Madrid Spain

5. Department Biochemistry and Physiology School of Pharmacy and Food Sciences Universitat de Barcelona Barcelona Spain

6. Department of Biochemistry and Molecular Biomedicine Faculty of Biology Universitat de Barcelona Barcelona Spain

7. School of Physics and Astronomy University of St Andrews North Haugh St Andrews Scotland

8. Department of Medicinal Chemistry Institute for Therapeutics Discovery and Development University of Minnesota Minneapolis MN 55414 USA

Abstract

AbstractThe family of dopamine D2‐like receptors represents an interesting target for a variety of neurological diseases, e. g. Parkinson's disease (PD), addiction, or schizophrenia. In this study we describe the synthesis of a new set of fluorescent ligands as tools for visualization of dopamine D2‐like receptors. Pharmacological characterization in radioligand binding studies identified UR‐MN212 (20) as a high‐affinity ligand for D2‐like receptors (pKi (D2longR)=8.24, pKi (D3R)=8.58, pKi (D4R)=7.78) with decent selectivity towards D1‐like receptors. Compound 20 is a neutral antagonist in a Go1 activation assay at the D2longR, D3R, and D4R, which is an important feature for studies using whole cells. The neutral antagonist 20, equipped with a 5‐TAMRA dye, displayed rapid association to the D2longR in binding studies using confocal microscopy demonstrating its suitability for fluorescence microscopy. Furthermore, in molecular brightness studies, the ligand's binding affinity could be determined in a single‐digit nanomolar range that was in good agreement with radioligand binding data. Therefore, the fluorescent compound can be used for quantitative characterization of native D2‐like receptors in a broad variety of experimental setups.

Funder

Fonds der Chemischen Industrie

Universität Regensburg

Elitenetzwerk Bayern

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

Organic Chemistry,Molecular Biology,Molecular Medicine,Biochemistry

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