RT Journal Article SR Electronic T1 Insights into the structure-activity relationship of glycosides as positive allosteric modulators acting on P2X7 receptors JF Molecular Pharmacology JO Mol Pharmacol FD American Society for Pharmacology and Experimental Therapeutics SP MOLPHARM-AR-2020-000129 DO 10.1124/molpharm.120.000129 A1 Waraporn Piyasirananda A1 Andrew Beekman A1 A. Ganesan A1 Stefan Bidula A1 Leanne Stokes YR 2020 UL http://molpharm.aspetjournals.org/content/early/2020/12/15/molpharm.120.000129.abstract AB P2X7 is an important ligand-gated ion channel expressed in multiple immune cell populations. This study aimed to investigate the chemical requirements of triterpenoid glycosides within a new binding pocket to characterise the structure-activity relationship. A set of glycosides were screened for positive modulator activity at human P2X7 using a YO-PRO-1 dye uptake assay in HEK-hP2X7 cells. The highest positive modulator activity was with ginsenoside CK, containing a monosaccharide (glucose) attached at carbon-20. Ginsenoside 20(S)Rg3, containing a disaccharide group (glucose-glucose) at carbon-3, displayed positive modulator activity with a reduced EC50 for ATP and increased maximal response at hP2X7. The epimer 20(R)Rg3 was inactive. A similar stereo-specific pattern was observed for 20(S)-Rh2. Ginsenoside-F1, highly similar to ginsenoside CK but containing a single additional hydroxyl group, was also inactive at P2X7. Computational docking suggests hydrophobic residues in the pocket are involved in steric discrimination between triterpenoids, while the position and identity of the carbohydrate group is important for positive modulator activity at human P2X7. Ginsenosides containing monosaccharide attachments perform better than di- or tri-saccharide glycosides. Additional modifications to the triterpenoid scaffold at carbon-6 are not tolerated. Gypenosides from plant sources other than Panax ginseng (gypenoside XVII, gypenoside XLIX, stevenleaf) can also act as positive allosteric modulators of P2X7. We also investigated the effect of positive allosteric modulators on endogenous P2X7 in THP-1 monocytes and confirmed our findings in a calcium response assay. A cell viability assay showed potentiation of ATP-induced cell death with ginsenoside CK in THP-1 and HEK-hP2X7 cells. Significance Statement Ginsenosides are active as PAMs at P2X7 and this study determines the chemical features important for mediating this effect. The position and identity of the sugar group is important for activity as is the position of a number of hydroxyl groups on the triterpenoid scaffold. Diastereomers of ginsenosides Rg3 and Rh2 demonstrate the importance of the location of hydroxyl groups relative to the hydrophobic face of the predicted binding pocket.