Studies on the molecular basis of H+ translocation by cytochromec oxidase |
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Authors: | Robert P. Casey Clemens Broger Marcus Thelen Angelo Azzi |
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Affiliation: | (1) Medizinisch-chemisches Institut der Universität Bern, Bühlstrasse 28, CH-3012 Bern, Switzerland |
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Abstract: | We report here studies which characterize further the interaction ofN,N-dicyclohexylcarbodiimide with cytochromec oxidase leading to inhibition of H+ translocation by the enzyme. Further evidence is presented to show that the inhibition results from a real interaction of DCCD with the enzyme and cannot be accounted for by uncoupling and, contrary to recent criticisms, this interaction occurs specifically with subunit III of the enzyme even at relatively high inhibitor-to-enzyme stoichiometries. Use of a spin-label analogue of DCCD has enabled us to demonstrate that the carbodiimide-binding site is highly apolar and may not lie on the pathway of electron transfer.Abbreviations DCCD N,N-dicyclohexylcarbodiimide - NCCD N-(2, 2, 6, 6-tetramethylpiperidyl-1-oxyl)-N-(cyclohexyl)carbodiimide - Hepes 2-(N-2-hydroxyethylpiperazin-N-yl) ethane sulfonate - TMPD N,N,N,N-tetramethylphenylenediamine |
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Keywords: | cytochrome oxidase mitochondria structure membrane protein subunits oxidation-reduction |
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