Calix[4]arene C-90 selectively inhibits Ca2+,Mg2+-ATPase of myometrium cell plasma membrane

The supramolecular compound calix[4]arene C-90 (5,11,17,23-tetra(trifluoro)methyl(phenylsulfonylimino)-methylamino-25,26,27,28-tetrapropoxycalix[4]arene) is shown to efficiently inhibit the ATP hydrolase activity of Ca 2+ ,Mg 2+ -ATPase in the myometrium cell plasma membrane fraction and also in a p...

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Published inBiochemistry (Moscow) Vol. 79; no. 5; pp. 417 - 424
Main Authors Veklich, T. A., Shkrabak, A. A., Slinchenko, N. N., Mazur, I. I., Rodik, R. V., Boyko, V. I., Kalchenko, V. I., Kosterin, S. A.
Format Journal Article
LanguageEnglish
Published Moscow Pleiades Publishing 01.05.2014
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Summary:The supramolecular compound calix[4]arene C-90 (5,11,17,23-tetra(trifluoro)methyl(phenylsulfonylimino)-methylamino-25,26,27,28-tetrapropoxycalix[4]arene) is shown to efficiently inhibit the ATP hydrolase activity of Ca 2+ ,Mg 2+ -ATPase in the myometrium cell plasma membrane fraction and also in a preparation of the purified enzyme solubilized from this subcellular fraction. The inhibition coefficient I 0.5 values were 20.2 ± 0.5 and 58.5 ± 6.4 μM for the membrane fraction and the solubilized enzyme, respectively. The inhibitory effect of calix[4]arene C-90 was selective comparatively to other ATPases localized in the plasma membrane: calix[4]arene C-90 did not influence the activities of Na + ,K + -ATPase and “basal” Mg 2+ -ATPase. The inhibitory effect of calix[4]arene C-90 on the Ca 2+ ,Mg 2+ -ATPase activity was associated with the cooperative action of four trifluoromethylphenyl sulfonylimine (sulfonylamidine) groups oriented similarly on the upper rim of the calix[4]arene macrocycle (the calix[4]arene “bowl”). The experimental findings seem to be of importance for studies, using calix[4]arene C-90, of membrane mechanisms of regulation of calcium homeostasis in smooth muscle cells and also for investigation of the participation of the plasma membrane Ca 2+ -pump in control of electro- and pharmacomechanical coupling in myocytes.
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ISSN:0006-2979
1608-3040
DOI:10.1134/S0006297914050058