Journal
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 61, Issue 22, Pages -Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202115545
Keywords
Adenosine A(2A) Receptor; Cancer; G Protein-Coupled Receptor (GPCR); Preladenant Conjugates; Protein Structures
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Funding
- Deutsche Forschungsgemeinschaft [SFB1328, FOR2372]
- German Federal Ministry of Research and Technology (BMBF)
- Fonds der Chemischen Industrie (FCI)
- Projekt DEAL
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Researchers developed a new A(2A)AR construct and successfully co-crystallized it with Preladenant derivatives, providing explanations for their high potency and selectivity through crystal structures. This study is of great importance for further research on class A GPCRs.
The G protein-coupled adenosine A(2A) receptor (A(2A)AR) is an important new (potential) drug target in immuno-oncology, and for neurodegenerative diseases. Preladenant and its derivatives belong to the most potent A(2A)AR antagonists displaying exceptional selectivity. While crystal structures of the human A(2A)AR have been solved, mostly using the A(2A)-StaR2 protein that bears 9 point mutations, co-crystallization with Preladenant derivatives has so far been elusive. We developed a new A(2A)AR construct harboring a single point mutation (S91(3.39)K) which renders it extremely thermostable. This allowed the co-crystallization of two novel Preladenant derivatives, the polyethylene glycol-conjugated (PEGylated) PSB-2113, and the fluorophore-labeled PSB-2115. The obtained crystal structures (2.25 angstrom and 2.6 angstrom resolution) provide explanations for the high potency and selectivity of Preladenant derivatives. They represent the first crystal structures of a GPCR in complex with PEG- and fluorophore-conjugated ligands. The applied strategy is predicted to be applicable to further class A GPCRs.
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