文章基本信息

标题：Identification of V6.51L as a selectivity hotspot in stereoselective A _2B adenosine receptor antagonist recognition
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作者：Xuesong Wang ; Willem Jespers ; Rubén Prieto-Díaz 等
期刊名称：Scientific Reports
电子版ISSN：2045-2322
出版年度：2021
卷号：11
DOI：10.1038/s41598-021-93419-x
语种：English
出版社：Springer Nature
摘要：The four adenosine receptors (ARs) A 1AR, A 2AAR, A 2BAR , and A 3AR are G protein-coupled receptors (GPCRs) for which an exceptional amount of experimental and structural data is available. Still, limited success has been achieved in getting new chemical modulators on the market. As such, there is a clear interest in the design of novel selective chemical entities for this family of receptors. In this work, we investigate the selective recognition of ISAM-140, a recently reported A 2BAR reference antagonist. A combination of semipreparative chiral HPLC, circular dichroism and X-ray crystallography was used to separate and unequivocally assign the configuration of each enantiomer. Subsequently affinity evaluation for both A 2A and A 2B receptors demonstrate the stereospecific and selective recognition of ( S)-ISAM140 to the A 2BAR. The molecular modeling suggested that the structural determinants of this selectivity profile would be residue V250 6.51 in A 2BAR, which is a leucine in all other ARs including the closely related A 2AAR. This was herein confirmed by radioligand binding assays and rigorous free energy perturbation (FEP) calculations performed on the L249V 6.51 mutant A 2AAR receptor. Taken together, this study provides further insights in the binding mode of these A 2BAR antagonists, paving the way for future ligand optimization.