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Studies on the molecular basis of H+ translocation by cytochromec oxidase
Authors:Robert P. Casey  Clemens Broger  Marcus Thelen  Angelo Azzi
Affiliation:(1) Medizinisch-chemisches Institut der Universität Bern, Bühlstrasse 28, CH-3012 Bern, Switzerland
Abstract:We report here studies which characterize further the interaction ofN,Nprime-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,Nprime-dicyclohexylcarbodiimide - NCCD N-(2, 2, 6, 6-tetramethylpiperidyl-1-oxyl)-Nprime-(cyclohexyl)carbodiimide - Hepes 2-(N-2-hydroxyethylpiperazin-Nprime-yl) ethane sulfonate - TMPD N,N,Nprime,Nprime-tetramethylphenylenediamine
Keywords:cytochrome  oxidase  mitochondria  structure membrane  protein  subunits  oxidation-reduction
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