Effect of hemolysate on calcium inhibition of the (Na+ + K+)-ATPase of human red blood cells |
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Authors: | D R Yingst M J Marcovitz |
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Affiliation: | Department of Physiology, Wayne State University School of Medicine, Detroit, Michigan 48201 USA |
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Abstract: | The sensitivity of the (Na+ + K+)-ATPase in human red cell membranes to inhibition by Ca2+ is markedly increased by the addition of diluted cytoplasm from hemolyzed human red blood cells. The concentration of Ca2+ causing 50% inhibition of the (Na+ + K+)-ATPase is shifted from greater than 50 microM free Ca2+ in the absence of hemolysate to less than 10 microM free Ca2+ when hemolysate diluted 1:60 compared to in vivo concentrations is added to the assay mixture. Boiling the hemolysate destroys its ability to increase the sensitivity of the (Na+ + K+)-ATPase to Ca2+. Proteins extracted from the membrane in the presence of EDTA and concentrated on an Amicon PM 30 membrane increased the sensitivity of the (Na+ + K+)-ATPase to Ca2+ in a dose-dependent fashion, causing over 80% inhibition of the (Na+ + K+)-ATPase at 10 microM free Ca2+ at the highest concentration of the extract tested. The active factor in this membrane extract is Ca2+-dependent, because it had no effect on the (Na+ + K+)-ATPase in the absence of Ca2+. Trypsin digestion prior to the assay destroyed the ability of this protein extract to increase the sensitivity of the (Na+ + K+)-ATPase to Ca2+. |
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Keywords: | Hepes N-2-hydroxyethylpiperazine-N′-2-ethanesulfonic acid EGTA ethyleneglycol-bis(β-aminoethyl ether)N,N′-tetraacetic acid EDTA ethylenediaminetetraacetic acid |
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