Kuznetsov 1996 J Biol Chem: Difference between revisions
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{{Publication | {{Publication | ||
|title=Kuznetsov AV, Clark JF, Winkler K, Kunz WS (1996) Increase of flux control of cytochrome c oxidase in copper-deficient mottled brindled mice. J | |title=Kuznetsov AV, Clark JF, Winkler K, Kunz WS (1996) Increase of flux control of cytochrome c oxidase in copper-deficient mottled brindled mice. J Biol Chem 271: 283-288. | ||
|info=[http://www.ncbi.nlm.nih.gov/pubmed/8550574 PMID: 8550574] | |info=[http://www.ncbi.nlm.nih.gov/pubmed/8550574 PMID: 8550574] | ||
|authors=Kuznetsov AV, Clark JF, Winkler K, Kunz WS | |authors=Kuznetsov AV, Clark JF, Winkler K, Kunz WS |
Revision as of 12:47, 14 December 2011
Kuznetsov AV, Clark JF, Winkler K, Kunz WS (1996) Increase of flux control of cytochrome c oxidase in copper-deficient mottled brindled mice. J Biol Chem 271: 283-288. |
ยป [[Has info::PMID: 8550574]]
Kuznetsov AV, Clark JF, Winkler K, Kunz WS (1996) J. Biol. Chem.
Abstract: The brindled mottled mouse (Mobr), an animal model of the Menkes' copper deficiency syndrome, was used for the investigation of changes in respiratory flux control associated with cytochrome c oxidase deficiency in muscle. Enzymatic analysis of cardiac and skeletal muscles showed an approximately 2-fold decrease in cytochrome c oxidase activity of brindled mutants in both types of muscles as compared with controls. The activities of NADH-cytochrome c oxidoreductase (respiratory chain segment I-III) and succinate-cytochrome c oxidoreductase (segment II-III) were normal. Assessment of mitochondrial respiratory function was performed using chemically skinned musculus quadriceps or heart muscle fibers isolated from control and brindled mottled mice. In skeletal muscle, there was no difference found in maximal rates of respiration. In the Mobr hearts, this parameter was slightly lower than control. Alternately, the determination of flux control coefficients of cytochrome c oxidase performed by a step by step inhibition of respiration with increasing concentrations of azide or cyanide revealed significantly sharper inhibition curves for brindled mice than for control, indicating more than 2-fold elevated flux control coefficients of cytochrome c oxidase. This investigation proved essential in characterizing the metabolic effect of a cytochrome c oxidase deficiency. We conclude, therefore, that application of metabolic control analysis can be a valuable approach to study defects of mitochondrial oxidative phosphorylation.
Labels:
Stress:Mitochondrial Disease; Degenerative Disease and Defect, Genetic Defect; Knockdown; Overexpression Organism: Mouse Tissue;cell: Cardiac Muscle, Skeletal Muscle Preparation: Permeabilized Cell or Tissue; Homogenate Enzyme: Complex IV; Cytochrome c Oxidase Regulation: Respiration; OXPHOS; ETS Capacity
HRR: Oxygraph-2k