Influence of 8-azido-ATP and other anions on the activity of cytochromec oxidase |
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Authors: | Fritz-Joachim Hüther Jan Berden Bernhard Kadenbach |
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Affiliation: | (1) Biochemie, Fachbereich Chemie der Philipps-Universität Hans-Meerwein-Strasse, D-3550 Marburg, FRG;(2) Laboratory of Biochemistry, University of Amsterdam, 1000 HD Amsterdam, Holland |
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Abstract: | ![]() The effect of ATP and other anions on the kinetics of cytochromec oxidation by reconstituted bovine heart cytochromec oxidase was investigated. The following results were obtained: (1) ATP and other polyvalent anions increase theKm for cytochromec and theVmax (if assayed by the photometric method). The magnitude of the effect is proportional to the charge of the anion as follows from the series of increasing effectiveness: Piii. (2) The kinetic effects are obtained in the millimolar physiological concentration range. (3) The kinetic changes are not saturated at high concentrations. (4) A specific interaction site for ATP at the cytosolic domain of the enzyme is concluded from the increase ofKm for cytochromec after photolabelling of proteoliposomes with 8-azido-[ -32P]-ATP, which is protected by ATP but not by ADP. (5) No specific binding site for ATP could be identified by photolabelling with 8-azido-[ -32P]-ATP. The labelling is only partly protected by ATP or ADP.Abbreviations CCP carbonylcyanide-m-chlorophenylhydrazone - TMPD N,N,N ,N -tetramethyl-1,4-phenylenediamine dihydrochloride - 8-N3-ATP 8-azido-adenosine-5 -triphosphateDedicated to Professor Dr. Friedhelm Schneider on the occasion of his 60th birthday. |
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Keywords: | Cytochromec oxidase enzyme kinetics photoaffinity labelling nucleotides proteoliposomes regulation of activity |
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