Abstract
(rmNa+ + K+)-ATPase from kidney outer medulla was incorporated into artificial dioleoylphosphatidylcholine vesicles. In the reconstituted system the pump can be activated by adding ATP to the external medium. ATP-driven potassium extrusion by the Na+,K+-pump was studied using a voltage-sensitive dye in the presence of valinomycin. ADP strongly reduced the turnover rate of the pump with a concentration for half-maximal inhibition of cD, 1 2 = 0.1 mM. cD, 1 2 was found to be virtually independent of ATP concentration, indicating that the inhibition is non-competitive with respect to ATP. The non-competitive inhibition by ADP can be explained on the basis of the Post-Albers reaction cycle of the Na+,K+-pump, assuming that the main action of ADP is the reversal of the phosphorylation step. A similar 'product inhibition' was observed with inorganic phosphate, but at much higher concentrations (cp, 1 2 = 14 mM). © 1986.
Original language | English |
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Pages (from-to) | 105-115 |
Number of pages | 10 |
Journal | Biochimica et Biophysica Acta - Biomembranes |
Volume | 857 |
Issue number | 1 |
Publication status | Published - 9 May 1986 |
Keywords
- (Na+ + K+)-ATPase
- (Rabbit kidney)
- Fluorescence
- Kinetics
- Membrane reconstitution
- Product inhibition