Effects of the ATP, ADP and inorganic phosphate on the transport rate of the Na+,K+-pump

H. J. Apell, M. T. Nelson, M. M. Marcus, P. Läuger

    Research output: Contribution to journalArticlepeer-review

    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 languageEnglish
    Pages (from-to)105-115
    Number of pages10
    JournalBiochimica et Biophysica Acta - Biomembranes
    Volume857
    Issue number1
    Publication statusPublished - 9 May 1986

    Keywords

    • (Na+ + K+)-ATPase
    • (Rabbit kidney)
    • Fluorescence
    • Kinetics
    • Membrane reconstitution
    • Product inhibition

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