Assembly factors and ATP-dependent proteases in cytochrome c oxidase biogenesis
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem, přehledy
PubMed
20398622
DOI
10.1016/j.bbabio.2010.04.006
PII: S0005-2728(10)00139-8
Knihovny.cz E-zdroje
- MeSH
- biologické modely MeSH
- lidé MeSH
- mitochondrie metabolismus MeSH
- molekulární chaperony metabolismus MeSH
- podjednotky proteinů MeSH
- proteasy závislé na ATP metabolismus MeSH
- respirační komplex IV biosyntéza chemie MeSH
- Saccharomyces cerevisiae metabolismus MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- přehledy MeSH
- Názvy látek
- molekulární chaperony MeSH
- podjednotky proteinů MeSH
- proteasy závislé na ATP MeSH
- respirační komplex IV MeSH
Eukaryotic cytochrome c oxidase (CcO), the terminal enzyme of the energy-transducing mitochondrial electron transport chain is a hetero-oligomeric, heme-copper oxidase complex composed of both mitochondrially and nuclear-encoded subunits. It is embedded in the inner mitochondrial membrane where it couples the transfer of electrons from reduced cytochrome c to molecular oxygen with vectorial proton translocation across the membrane. The biogenesis of CcO is a complicated sequential process that requires numerous specific accessory proteins, so-called assembly factors, which include translational activators, translocases, molecular chaperones, copper metallochaperones and heme a biosynthetic enzymes. Besides these CcO-specific protein factors, the correct biogenesis of CcO requires an even greater number of proteins with much broader substrate specificities. Indeed, growing evidence indicates that mitochondrial ATP-dependent proteases might play an important role in CcO biogenesis. Out of the four identified energy-dependent mitochondrial proteases, three were shown to be directly involved in proteolysis of CcO subunits. In addition to their well-established protein-quality control function these oligomeric proteolytic complexes with chaperone-like activities may function as molecular chaperones promoting productive folding and assembly of subunit proteins. In this review, we summarize the current knowledge of the functional involvement of eukaryotic CcO-specific assembly factors and highlight the possible significance for CcO biogenesis of mitochondrial ATP-dependent proteases.
Citace poskytuje Crossref.org
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