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Mitofilin complexes: conserved organizers of mitochondrial membrane architecture
- Source :
- bchm. 393:1247-1261
- Publication Year :
- 2012
- Publisher :
- Walter de Gruyter GmbH, 2012.
-
Abstract
- Mitofilin proteins are crucial organizers of mitochondrial architecture. They are located in the inner mitochondrial membrane and interact with several protein complexes of the outer membrane, thereby generating contact sites between the two membrane systems of mitochondria. Within the inner membrane, mitofilins are part of hetero-oligomeric protein complexes that have been termed the mitochondrial inner membrane organizing system (MINOS). MINOS integrity is required for the maintenance of the characteristic morphology of the inner mitochondrial membrane, with an inner boundary region closely apposed to the outer membrane and cristae membranes, which form large tubular invaginations that protrude into the mitochondrial matrix and harbor the enzyme complexes of the oxidative phosphorylation machinery. MINOS deficiency comes along with a loss of crista junction structures and the detachment of cristae from the inner boundary membrane. MINOS has been conserved in evolution from unicellular eukaryotes to humans, where alterations of MINOS subunits are associated with multiple pathological conditions.
- Subjects :
- DOMINANT OPTIC ATROPHY
Translocase of the outer membrane
Clinical Biochemistry
Muscle Proteins
Biology
Models, Biological
Biochemistry
Mitochondrial Proteins
mitochondrial morphology
Mitochondrial membrane transport protein
CRISTAE MORPHOLOGY
ELECTRON TOMOGRAPHY
cristae
INNER-MEMBRANE
PROTEIN IMPORT
Animals
Humans
PROTEOMIC IDENTIFICATION
Inner membrane
DYNAMIN-RELATED GTPASE
OXIDATIVE STRESS
Inner mitochondrial membrane
Molecular Biology
Conserved Sequence
Fcj1
MINOS
TRANSLOCATION CONTACT SITES
MICOS complex
crista junction
Mitochondrial carrier
Cell biology
Mio10
Mitochondrial Membranes
RAT-BRAIN MITOCHONDRIA
Translocase of the inner membrane
biology.protein
Bacterial outer membrane
Subjects
Details
- ISSN :
- 14374315 and 14316730
- Volume :
- 393
- Database :
- OpenAIRE
- Journal :
- bchm
- Accession number :
- edsair.doi.dedup.....a0f852fd744f3a491d1895ffd87257e3
- Full Text :
- https://doi.org/10.1515/hsz-2012-0239