Jespers, WillemVerdon, GrégoryAzuaje, JhonnyMajellaro, MaríaKeränen, HenrikGarcía Mera, XerardoCongreve, MilesDeflorian, FrancescaDe Graaf, ChrisZhukov, AndreyDoré, Andrew S.Mason, Jonathan S.Åqvist, JohanCooke, Robert M.Sotelo Pérez, EddyGutiérrez de Terán, Hugo2024-02-072024-02-072020Jespers, W., Verdon, G., Azuaje, J., Majellaro, M., Keränen, H., García-Mera, X., Congreve, M., Deflorian, F., de Graaf, C., Zhukov, A., Doré, A.S., Mason, J.S., Åqvist, J., Cooke, R.M., Sotelo, E., Gutiérrez-de-Terán, H. (2020). X-Ray Crystallography and Free Energy Calculations Reveal the Binding Mechanism of A2A Adenosine Receptor Antagonists. "Angewandte Chemie International Edition", vol. 59, 16536-16553http://hdl.handle.net/10347/32497We present a robust protocol based on iterations of free energy perturbation (FEP) calculations, chemical synthesis, biophysical mapping and X-ray crystallography to reveal the binding mode of an antagonist series to the adenosine A2A receptor (AR). Eight A2AAR binding site mutations from biophisical mapping experiments were initially analysed with sidechain FEP simulations, performed on alternate binding modes. The results distinctively supported one binding mode, which was subsequently used to design new chromone derivatives. Their affinities for the A2AAR were experimentally determined and investigated through a cycle of ligandFEP calculations, validating the binding orientation of the different chemical substituents proposed. Subsequent X-ray crystallography of the A2AAR with a low and a high affinity chromone derivative confirmed the predicted binding orientation. The new molecules and structures here reported were driven by free energy calculations, and provide new insights on antagonist binding to the A2AAR, an emerging target in immuno-oncology.engCC BY 4.0http://creativecommons.org/licenses/by-nc-nd/4.0/Adenosine receptorsBiophysical mapping (BPM)Free energy perturbation (FEP)G protein-coupled receptor (GPCR)2406 Biofísica2306 Química orgánicajournal article10.1002/anie.2020037881521-3773open access