Significance of respirasomes for the assembly/stability of human respiratory chain complex I

被引:246
作者
Schägger, H
de Coo, R
Bauer, MF
Hofmann, S
Godinot, C
Brandt, U
机构
[1] Goethe Univ Frankfurt, Fachbereich Med, Zentrum Biol Chem, Inst Biochem 1, D-60590 Frankfurt, Germany
[2] Erasmus Univ, Med Ctr, Dept Neurol, NL-3000 DR Rotterdam, Netherlands
[3] Acad Hosp Munich Schwabing, Inst Clin Chem Mol Diagnost & Mitochondrial Genet, D-80804 Munich, Germany
[4] Acad Hosp Munich Schwabing, Diabet Res Inst, D-80804 Munich, Germany
[5] Ctr Mol & Cell Genet, CNRS, Unit 5534, F-69622 Villeurbanne, France
[6] Univ Lyon 1, F-69622 Villeurbanne, France
关键词
D O I
10.1074/jbc.M404033200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We showed that the human respiratory chain is organized in supramolecular assemblies of respiratory chain complexes, the respirasomes. The mitochondrial complexes I (NADH dehydrogenase) and III (cytochrome c reductase) form a stable core respirasome to which complex IV (cytochrome c oxidase) can also bind. An analysis of the state of respirasomes in patients with an isolated deficiency of single complexes provided evidence that the formation of respirasomes is essential for the assembly/stability of complex I, the major entry point of respiratory chain substrates. Genetic alterations leading to a loss of complex III prevented respirasome formation and led to the secondary loss of complex I. Therefore, primary complex III assembly deficiencies presented as combined complex III/I defects. This dependence of complex I assembly/stability on respirasome formation has important implications for the diagnosis of mitochondrial respiratory chain disorders.
引用
收藏
页码:36349 / 36353
页数:5
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