Abstract
(Na + + K +)-ATPase from shark rectal glands reconstituted into lipid vesicles and oriented inside out catalyses an ouabain-sensitive Na +Na + exchange in the absence of intravesicular K + when ATP is added extravesicularly. Intravesicular ouabain inhibited the exchange completely. This was also the case with digitoxigenin added to the vesicles. Intravesicular oligomycin inhibited the Na +Na + exchange partly in a fashion which was ATP dependent. The exchange is accompanied by a net hydrolysis of ATP with an apparent K m of 2.5 μM. ADP was found to give no stimulation of the Na +Na + exchange, contrarily, ADP inhibited the ATP-dependent exchange of Na + both at optimal and supraoptimal ATP concentrations. When initial influx and efflux of 22Na was measured and the hydrolysis of ATP concomitantly determined a coupling ratio of 2.8:1.3:1 was found, i.e. 2.8 moles of Na + were taken up (cellular efflux) and 1.3 moles of Na + extruded (cellular influx) for each mole of ATP hydrolyzed. The electrogenic Na +Na + exchange generated a transmembrane potential which was measured with the fluorescent probe ANS (8-anilino-1-naphthalenesulfonic acid) to be 60 mV positive inside the liposomes (extracellular).
Published Version
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