Biophysical Dissection of Isolated GPCRs: The Adenosine A2A Receptor under the Bistouries

Author:

Banères Jean-Louis1,Botzanowski Thomas2,Boutin Jean A.3ORCID,Calamini Barbara4ORCID,Castel Jérôme25,Catoire Laurent J.6ORCID,Cianférani Sarah2ORCID,Demesmay Claire7,Ferguson Gavin8ORCID,Ferry Gilles9,Kniazeff Julie1,Krimm Isabelle10ORCID,Langer Thierry11ORCID,Lebon Guillaume8,Ley Marie2ORCID,Nyerges Miklos12ORCID,Schwob Magali513,Venien-Bryan Catherine14,Wagner Renaud13,Zeder-Lutz Gabrielle13,Zilian-Stohrer Claudia6

Affiliation:

1. Institut des Biomolécules Max Mousseron (IBMM), UMR 5247, CNRS-Université de Montpellier-ENSCM, 34093 Montpellier, France

2. Laboratoire de Spectrométrie de Masse BioOrganique (LSMBO), Institut Pluridisciplinaire Hubert Curien, IPHC, CNRS UMR 7178, Infrastructure Nationale de Protéomique ProFI, FR 2048 CNRS CEA, Université de Strasbourg, 67084 Strasbourg, France

3. Laboratory of Neuroendocrine Endocrine and Germinal Differentiation and Communication (NorDiC), Université de Rouen Normandie, Inserm, UMR 1239, 76000 Rouen, France

4. Center for Drug Discovery, Department of Neurobiology, Duke University Medical Center, Durham, NC 27710, USA

5. Department of Structural Biology, NovAliX, 67080 Strasbourg, France

6. Laboratoire de Biologie Physico-Chimique des Protéines Membranaires, UMR 7099, IBPC, 75005 Paris, France

7. Equipe Techsep, Institut des Sciences Analytiques, 69100 Villeurbanne, France

8. Institut de Génomique Fonctionnelle, Université de Montpellier, CNRS, INSERM, 34094 Montpellier, France

9. Institut de Recherches Servier, 78290 Croissy-sur-Seine, France

10. Small Molecules for Biological Targets Team, Université Claude Bernard Lyon 1, INSERM 1052, CNRS 5286, Centre Léon Bérard, Centre de Recherche en Cancérologie de Lyon, 69373 Lyon, France

11. Department of Pharmaceutical Sciences, University of Vienna, 1090 Vienna, Austria

12. Servier Research Institute of Medicinal Chemistry, 1031 Budapest, Hungary

13. Plateforme IMPReSs, UMR 7242, Biotechnologie et Signalisation Cellulaire, Ecole Supérieure de Biotechnologie de Strasbourg, 67412 Illkirch, France

14. Institut de Minéralogie, de Physique des Matériaux et de Cosmochimie, UMR 7590 CNRS, UPMC, IRD, MNHN, 75005 Paris, France

Abstract

In an effort to provide an overview of the biophysical approaches used to study G-protein-coupled receptors, we chose to consider the adenosine A2A receptor as a model, as it is widely reported in the literature to explore the way GPCRs are studied nowadays. After a brief introduction of the receptor, we gathered descriptions of the various tools used to investigate the pharmacology and structure of the A2A receptor. We began by describing the key developments which have led to successful studies of GPCRs including the cloning, expression and purification of A2A, and the subsequent characterizations including quality control, binding and functional studies that have been necessary for the further understanding of the receptor. Then, we reviewed the reconstitution of A2A into nanodiscs as well as the use of this biological material in structural mass spectrometry, NMR, calorimetry and various other approaches to gain not only information about the structure and function of A2A, but also the dynamics of the receptor and the tools necessary to pursue such investigations. The body of techniques presented herein are applicable to all GPCRs amenable to purification.

Publisher

MDPI AG

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