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Molecular Pharmacology, Vol 15, 620-626, Copyright © 1979 by the American Society for Pharmacology and Experimental Therapeutics
1 Department of Pharmacology, University of Alberta, Edmonton, Alberta, T6G 2H7 Canada
Although the harmala alkaloids were originally reported to be specific inhibitors of the Na+-activation site of (Na+ + K+)-ATPase, their reaction is now known to be more complex as the K+-activation site of this enzyme is also thought to be involved. By using a fluorescent method of assay employing 3-O-methyl fluorescein phosphate as substrate, and by appropriate correction of the data for the fluorescence quenching of harmaline itself, we have confirmed that this alkaloid directly interacts with the K+ activation site of the acyl-phosphatase partial reaction of (Na+ + K+)-ATPase. However, calculation of the Hill coefficients for harmaline inhibition of K+-acyl phosphatase and for K+-activation of the system in the presence of harmaline suggests that activation and inhibition do not occur at the same site.
Submitted on June 14, 1978