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Difference between revisions of "Pecina 2003 Biochim Biophys Acta"

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|abstract=Subacute necrotising encephalomyopathy (Leigh syndrome) due to cytochrome c oxidase (CIV; COX) deficiency is often caused by mutations in the ''SURF1'' gene, encoding the Surf1 protein essential for CIV assembly. We have investigated five patients with different ''SURF1''  mutations resulting in the absence of Surf1 protein. All of them presented with severe and generalised CIV defect. Immunoelectrophoretic analysis of cultured fibroblasts revealed 85% decrease of the normal-size CIV complexes and significant accumulation of incomplete COX assemblies of 90–120 kDa. Spectrophotometric assay of CIV activity showed a 70–90% decrease in lauryl maltoside (LM)-solubilised fibroblasts. In contrast, oxygen consumption analysis in whole cells revealed only a 13–31% decrease of COX activity, which was completely inhibited by detergent in patient cells but not in controls. In patient fibroblasts ADP-stimulated respiration was 50% decreased and cytofluorometry showed a significant decrease of mitochondrial membrane potential ΔΨm in [[State 4]], as well as a 2.4-fold higher sensitivity of ΔΨm  to uncoupler. We conclude that the absence of the Surf1 protein leads to the formation of incomplete CIV complexes, which ''in situ'' maintain rather high electron-transport activity, while their H<sub>+</sub>-pumping is impaired. Enzyme inactivation by the detergent in patient cells indicates instability of incomplete CIV assemblies.
|abstract=Subacute necrotising encephalomyopathy (Leigh syndrome) due to cytochrome c oxidase (CIV; COX) deficiency is often caused by mutations in the ''SURF1'' gene, encoding the Surf1 protein essential for CIV assembly. We have investigated five patients with different ''SURF1''  mutations resulting in the absence of Surf1 protein. All of them presented with severe and generalised CIV defect. Immunoelectrophoretic analysis of cultured fibroblasts revealed 85% decrease of the normal-size CIV complexes and significant accumulation of incomplete COX assemblies of 90–120 kDa. Spectrophotometric assay of CIV activity showed a 70–90% decrease in lauryl maltoside (LM)-solubilised fibroblasts. In contrast, oxygen consumption analysis in whole cells revealed only a 13–31% decrease of COX activity, which was completely inhibited by detergent in patient cells but not in controls. In patient fibroblasts ADP-stimulated respiration was 50% decreased and cytofluorometry showed a significant decrease of mitochondrial membrane potential ΔΨm in [[State 4]], as well as a 2.4-fold higher sensitivity of ΔΨm  to uncoupler. We conclude that the absence of the Surf1 protein leads to the formation of incomplete CIV complexes, which ''in situ'' maintain rather high electron-transport activity, while their H<sub>+</sub>-pumping is impaired. Enzyme inactivation by the detergent in patient cells indicates instability of incomplete CIV assemblies.
|keywords=Cytochrome ''c'' oxidase, ''SURF1'', Leigh syndrome, Mitochondrial disorder
|keywords=Cytochrome ''c'' oxidase, ''SURF1'', Leigh syndrome, Mitochondrial disorder
|mipnetlab=CZ_Prague_Zeman J, CZ_Prague_Houstek J, CZ Hradec Kralove Cervinkova Z
|mipnetlab=CZ Prague Zeman J, CZ Prague Houstek J, CZ Hradec Kralove Cervinkova Z
|discipline=Biomedicine
|discipline=Biomedicine
}}
}}

Revision as of 15:43, 24 March 2015

Publications in the MiPMap
Pecina P, Capkova M, Chowdhury SKR, Drahota Z, Dubot A, Vojtiskova A, Hansikova H, Houstekova H, Zeman J, Godinot C, Houstek J (2003) Functional alteration of cytochrome c oxidase by SURF1 mutations in Leigh syndrome. Biochim Biophys Acta 1639:53-63.

» PMID: 12943968

Pecina P, Capkova M, Chowdhury SKR, Drahota Z, Dubot A, Vojtiskova A, Hansikova H, Houstekova H, Zeman J, Godinot C, Houstek J (2003) Biochim Biophys Acta

Abstract: Subacute necrotising encephalomyopathy (Leigh syndrome) due to cytochrome c oxidase (CIV; COX) deficiency is often caused by mutations in the SURF1 gene, encoding the Surf1 protein essential for CIV assembly. We have investigated five patients with different SURF1 mutations resulting in the absence of Surf1 protein. All of them presented with severe and generalised CIV defect. Immunoelectrophoretic analysis of cultured fibroblasts revealed 85% decrease of the normal-size CIV complexes and significant accumulation of incomplete COX assemblies of 90–120 kDa. Spectrophotometric assay of CIV activity showed a 70–90% decrease in lauryl maltoside (LM)-solubilised fibroblasts. In contrast, oxygen consumption analysis in whole cells revealed only a 13–31% decrease of COX activity, which was completely inhibited by detergent in patient cells but not in controls. In patient fibroblasts ADP-stimulated respiration was 50% decreased and cytofluorometry showed a significant decrease of mitochondrial membrane potential ΔΨm in State 4, as well as a 2.4-fold higher sensitivity of ΔΨm to uncoupler. We conclude that the absence of the Surf1 protein leads to the formation of incomplete CIV complexes, which in situ maintain rather high electron-transport activity, while their H+-pumping is impaired. Enzyme inactivation by the detergent in patient cells indicates instability of incomplete CIV assemblies. Keywords: Cytochrome c oxidase, SURF1, Leigh syndrome, Mitochondrial disorder

O2k-Network Lab: CZ Prague Zeman J, CZ Prague Houstek J, CZ Hradec Kralove Cervinkova Z


Labels: MiParea: Respiration, nDNA;cell genetics, mt-Medicine, Patients  Pathology: Inherited 

Organism: Human 

Preparation: Intact cells, Permeabilized cells  Enzyme: Complex IV;cytochrome c oxidase  Regulation: Coupling efficiency;uncoupling, mt-Membrane potential, Uncoupler  Coupling state: LEAK, ROUTINE, OXPHOS, ETS"ETS" is not in the list (LEAK, ROUTINE, OXPHOS, ET) of allowed values for the "Coupling states" property. 

HRR: Oxygraph-2k