S Yuan*, H.C. S. Chan, H Vogel, S Filipek, R. C. Stevens* and K. Palczewski*

Angew. Chem. Int. Ed. (2016) 10.1002/ange.201605147, First published: 27 July 2016

Abstract

Human purinergic G protein-coupled receptor P2Y₁ (P2Y₁R) is activated by adenosine 5'-diphosphate (ADP) to induce platelet activation and thereby serves as an important antithrombotic drug target. Crystal structures of P2Y₁R revealed that one ligand (MRS2500) binds to the extracellular vestibule of this GPCR, whereas another (BPTU) occupies the surface between transmembrane (TM) helices TM2 and TM3. We introduced a total of 20 μs all-atom long-timescale molecular dynamic (MD) simulations to inquire why two molecules in completely different locations both serve as antagonists while ADP activates the receptor. Our results indicate that BPTU acts as an antagonist by stabilizing extracellular helix bundles leading to an increase of the lipid order, whereas MRS2500 blocks signaling by occupying the ligand binding site. Both antagonists stabilize an ionic lock within the receptor. However, binding of ADP breaks this ionic lock, forming a continuous water channel that leads to P2Y₁R activation.

Figure legend: Molecular mechanism of action inferred from the P2Y₁R structure. Left panel: Antagonist molecule BPTU binds to P2Y₁R and stablizes the ionic lock between K46^1.46 and R195^ECL2 via a decrease in the lipid order. No continuous internal water channel is formed. Middle panel: Antagonist molecule MRS2500 binds to P2Y₁R and stablizes the ionic lock between K46^1.46 and R195^ECL2.  No water continuous internal water channel is formed. Right panel: Agonist molecule ADP binds to P2Y₁R and disrupts the ionic lock between K46^1.46 and R195^ECL2.  Y324^7.53 undergoes a molecular switch that results in the formation of a continuous water channel inside the receptor.

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