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  • Title: Pre-steady state kinetics of ATP hydrolysis by Na,K-ATPase.
    Author: Manzoor N, Haque MM, Khan LA.
    Journal: Cell Biochem Funct; 2009 Apr; 27(3):135-41. PubMed ID: 19277993.
    Abstract:
    Fast reaction kinetics of ATP hydrolysis by Na,K-ATPase has been investigated by following absorption pattern of pH sensitive dye in stopped flow spectrophotometer. Distinct pre-steady state phase signal could be recorded with an initial decrease in acidity followed by increase in acidity. Average half time for H(+) absorption and peak alkalinity was, respectively, 30 ms and 60 ms. Under optimal Na(+) (120 mM) and K(+) (30 mM) concentrations, magnitude of both H(+) absorption and H(+) release are found to be about 1.0 H(+)/ATPase molecule. H(+) absorption and release decreased with decrease in Na(+) concentration, H(+) release was more affected. Both H(+) absorption and H(+) release are found to be independent of K(+) concentration in the pre-steady state phase. No H(+) absorption or release was observed following mixing of either ADP, Na(+) or K(+) alone with ATPase. Effect of delayed mixing of Na(+) or K(+) on two phases of pre-steady state cycle indicates that ATP hydrolytic cycle starts without K(+) ions if optimal Na(+) is present. ATP hydrolytic cycle does not start in the absence of Na(+) ions. Results obtained have been interpreted in terms of an extended kinetic scheme for Na,K-ATPase.
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