TY - JOUR
T1 - Electrogenic H+ translocation by the plasma membrane ATPase of Neurospora. Studies on plasma membrane vesicles and reconstituted enzyme
AU - Perlin, D. S.
AU - Kasamo, K.
AU - Brooker, R. J.
AU - Slayman, C. W.
N1 - Copyright:
Copyright 2004 Elsevier B.V., All rights reserved.
PY - 1984
Y1 - 1984
N2 - 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.
AB - 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.
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M3 - Article
C2 - 6234306
AN - SCOPUS:0021280111
SN - 0021-9258
VL - 259
SP - 7884
EP - 7892
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 12
ER -