CCCP activation of the reconstituted NaK-pump

Summary

In the NaK-ATPase proteoliposomes (PLs), the NaK-pump activity, Na⁺ uptake, and ATP hydrolysis were apparently enhanced by carbonyl cyanidem-chlorophenylhydrazone (CCCP) and other ionophores without ion gradients. These ionophore effects were not cation specific. Without ionophores, the PL's ATPase activity fell to its steady-state value within 3 sec at 15°C. This decrease in activity disappeared in the presence of CCCP. Since CCCP is believed to enhance proton mobility across the lipid bilayer and dissipate membrane potential (V _m ), we postulated that aV _m build-up partially inhibits the PLs by changing the conformation of the NaK-pump, and that CCCP eliminated this partial inhibition. Since this activation required extracellular K⁺ and high ATP concentration in the PLs, CCCP must affect the conversion between the phosphorylated forms of NaK-ATPase (EP); this step has been suggested by Goldschlegger et al. (1987) to be the voltage-sensitive step (J. Physiol. (London) 387:331–355). Although cytoplasmic K⁺ accelerated the change of ADP-and K⁺-sensitive EP (E^*P) to K⁺-sensitive ADP-insensitive EP (E₂P), CCCP did not compete with cytoplasmic K⁺ when cytoplasmic Na⁺ was saturated. When the PLs were phosphorylated with 20 μm ATP and 20 μm palmitoyl CoA instead of with high concentration of ATP, CCCP increased the E^*P content and decreased the ADP-sensitive K⁺-insensitive EP (E₁P). The results described above suggest that CCCP affects the E₁P to E^*P change in the E₁P→E^*P→E₂P conversion and that this reaction step is inhibited byV _m .