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Originally published as Biophys J. BioFAST on May 9, 2008.
doi:10.1529/biophysj.108.133546
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Biophysical Journal 95:1813-1825 (2008)
© 2008 The Biophysical Society

Effect of Clotrimazole on the Pump Cycle of the Na,K-ATPase

Gianluca Bartolommei *, Nadège Devaux {dagger}, Francesco Tadini-Buoninsegni *, MariaRosa Moncelli * and Hans-Jürgen Apell {dagger}

* Department of Chemistry, University of Florence, Florence, Italy; and {dagger} Department of Biology, University of Konstanz, Konstanz, Germany

Correspondence: Address reprint requests to Hans-Jürgen Apell, E-mail: h-j.apell{at}uni-konstanz.de

The effect of the antimycotic drug clotrimazole (CLT) on the Na,K-ATPase was investigated using fluorescence and electrical measurements. The results obtained by steady-state fluorescence experiments with the electrochromic styryl dye RH421 were combined with those achieved by a pre-steady-state method based on fast solution exchange on a solid supported membrane that adsorbs the protein. Both techniques are suitable for monitoring the electrogenic steps of the pump cycle and are in general complementary, yielding distinct kinetic information. The experiments show clearly that CLT affects specific partial reactions of the pump cycle of the Na,K-ATPase with an affinity in the low micromolar range and in a reversible manner. All results can be consistently explained by proposing the CLT-promoted formation of an ion-occluded-CLT-bound conformational E2 state, Formula that acts as a "dead-end" side track of the pump cycle, where X stands for H+ or K+. Na+ binding, enzyme phosphorylation, and Na+ transport were not affected by CLT, and at high CLT concentrations ~1/3 of the enzyme remained active in the physiological transport mode. The presence of Na+ and K+ destabilized the inactivated form of the Na,K-ATPase.







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Copyright © 2008 by the Biophysical Society.