Fluorescent probes have been used to measure electrogenic proton pumping by the plasma membrane ATPase of Neurospora. In isolated plasma membrane vesicles, >85% of which are inverted, ATP hydrolysis is accompanied by the formation of an inside acid pH gradient (ΔpH) which can be detected by acridine orange fluorescence quenching and an inside positive membrane potential (ΔΨ) which can be detected by oxonol V fluorescence quenching. Maximal values of ΔpH were generated in the presence of a permeant anion (SCN-, NO3-, or Cl-) and maximal ΔΨ, in the absence of such anions. Cation effects were much less pronounced and can approximately be accounted for by nonspecific salt effects on the rate of ATP hydrolysis. In addition, a rapid method is described for the reconstitution of the [H+]-ATPase, starting from isolated plasma membranes. When the membranes are solubilized with deoxycholate in the presence of asolectin and detergent is removed by passage through a BioGel P-10 column, vesicles are reformed in which the M(r) = 104,000 polypeptide of the ATPase constitutes 35% of the protein. Freeze-fracture electron microscopy of the vesicles has revealed intramembrane particles with a diameter of 116 Å, equally distributed between the two fracture faces. Measurements with acridine orange and oxonol V indicate that the reconstituted ATPase retains its transport activity, generating both ΔpH and ΔΨ during the hydrolysis of MgATP.
|Original language||English (US)|
|Number of pages||9|
|Journal||Journal of Biological Chemistry|
|State||Published - 1984|
All Science Journal Classification (ASJC) codes
- Molecular Biology
- Cell Biology