The P-type ATPase inhibiting potential of polyoxotungstates

Polyoxometalates (POMs) are transition metal complexes that exhibit a broad diversity of structures and properties rendering them promising for biological purposes. POMs are able to inhibit a series of biologically important enzymes, including phosphatases, and thus are able to affect many biochemical processes. In the present study, we analyzed and compared the inhibitory effects of nine different polyoxotungstates (POTs) on two P-type ATPases, Ca(2+)-ATPase from skeletal muscle and Na(+)/K(+)-ATPase from basal membrane of skin epithelia. For Ca(2+)-ATPase inhibition, an in vitro study was performed and the strongest inhibitors were determined to be the large heteropolytungstate K(9)(C(2)H(8)N)(5)[H(10)Se(2)W(29)O(103)] (Se(2)W(29)) and the Dawson-type POT K(6)[α-P(2)W(18)O(62)] (P(2)W(18)) exhibiting IC(50) values of 0.3 and 0.6 μM, respectively. Promising results were also shown for the Keggin-based POTs K(6)H(2)[CoW(11)TiO(40)] (CoW(11)Ti, IC(50) = 4 μM) and Na(10)[α-SiW(9)O(34)] (SiW(9), IC(50) = 16 μM), K(14)[As(2)W(19)O(67)(H(2)O)] (As(2)W(19), IC(50) = 28 μM) and the lacunary Dawson K(12)[α-H(2)P(2)W(12)O(48)] (P(2)W(12), IC(50) = 11 μM), whereas low inhibitory potencies were observed for the isopolytungstate Na(12)[H(4)W(22)O(74)] (W(22), IC(50) = 68 μM) and the Anderson-type Na(6)[TeW(6)O(24)] (TeW(6), IC(50) = 200 μM). Regarding the inhibition of Na(+)/K(+)-ATPase activity, for the first time an ex vivo study was conducted using the opercular epithelium of killifish in order to investigate the effects of POTs on the epithelial chloride secretion. Interestingly, 1 μM of the most potent Ca(2+)-ATPase inhibitor, Se(2)W(29), showed only a minor inhibitory effect (14% inhibition) on Na(+)/K(+)-ATPase activity, whereas almost total inhibition (99% inhibition) was achieved using P(2)W(18). The remaining POTs exhibited similar inhibition rates on both ATPases. These results reveal the high potential of some POTs to act as P-type ATPase inhibitors, with Se(2)W(29) showing high selectivity towards Ca(2+)-ATPase.