Binding of ouabain and marinobufagenin leads to different structural changes in Na,K‐ATPase and depends on the enzyme conformation

Е. А. Климанова(Engelhardt Institute of Molecular Biology), Irina Yu. Petrushanko(Engelhardt Institute of Molecular Biology), Vladimir A. Mitkevich(Engelhardt Institute of Molecular Biology), Anastasia A. Anashkina(Engelhardt Institute of Molecular Biology), S.N. Orlov(Lomonosov Moscow State University), Alexander Makarov(Engelhardt Institute of Molecular Biology), O. D. Lopina(Lomonosov Moscow State University)
FEBS Letters
August 20, 2015
Cited by 41Open Access
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Abstract

Ion pump, Na,K-ATPase specifically binds cardiotonic steroids (CTS), which leads to inhibition of the enzyme activity and activation of signaling network in the cell. We have studied interaction of Na,K-ATPase with CTS of two different types - marinobufagenin and ouabain. We have shown that both CTS inhibit activity of Na,K-ATPase with the same Ki values, but binding of ouabain is sensitive to the conformation of Na,K-ATPase while binding of marinobufagenin is not. Furthermore, binding of ouabain and marinobufagenin results in different structural changes in Na,K-ATPase. Our data allow to explain the diversity of effects on the receptor function of Na,K-ATPase caused by different types of CTS.


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