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Iron-dependent self-assembly of recombinant yeast frataxin: implications for Friedreich ataxia.
- Source :
-
American journal of human genetics [Am J Hum Genet] 2000 Sep; Vol. 67 (3), pp. 549-62. Date of Electronic Publication: 2000 Aug 04. - Publication Year :
- 2000
-
Abstract
- Frataxin deficiency is the primary cause of Friedreich ataxia (FRDA), an autosomal recessive cardiodegenerative and neurodegenerative disease. Frataxin is a nuclear-encoded mitochondrial protein that is widely conserved among eukaryotes. Genetic inactivation of the yeast frataxin homologue (Yfh1p) results in mitochondrial iron accumulation and hypersensitivity to oxidative stress. Increased iron deposition and evidence of oxidative damage have also been observed in cardiac tissue and cultured fibroblasts from patients with FRDA. These findings indicate that frataxin is essential for mitochondrial iron homeostasis and protection from iron-induced formation of free radicals. The functional mechanism of frataxin, however, is still unknown. We have expressed the mature form of Yfh1p (mYfh1p) in Escherichia coli and have analyzed its function in vitro. Isolated mYfh1p is a soluble monomer (13,783 Da) that contains no iron and shows no significant tendency to self-associate. Aerobic addition of ferrous iron to mYfh1p results in assembly of regular spherical multimers with a molecular mass of approximately 1. 1 MDa (megadaltons) and a diameter of 13+/-2 nm. Each multimer consists of approximately 60 subunits and can sequester >3,000 atoms of iron. Titration of mYfh1p with increasing iron concentrations supports a stepwise mechanism of multimer assembly. Sequential addition of an iron chelator and a reducing agent results in quantitative iron release with concomitant disassembly of the multimer, indicating that mYfh1p sequesters iron in an available form. In yeast mitochondria, native mYfh1p exists as monomer and a higher-order species with a molecular weight >600,000. After addition of (55)Fe to the medium, immunoprecipitates of this species contain >16 atoms of (55)Fe per molecule of mYfh1p. We propose that iron-dependent self-assembly of recombinant mYfh1p reflects a physiological role for frataxin in mitochondrial iron sequestration and bioavailability.
- Subjects :
- Chromatography, Gel
Escherichia coli genetics
Friedreich Ataxia enzymology
Friedreich Ataxia genetics
Homeostasis
Humans
Iron analysis
Iron metabolism
Iron Chelating Agents pharmacology
Microscopy, Atomic Force
Microscopy, Electron
Mitochondria enzymology
Mitochondria metabolism
Models, Biological
Molecular Sequence Data
Molecular Weight
Oxidative Stress
Phosphotransferases (Alcohol Group Acceptor) chemistry
Phosphotransferases (Alcohol Group Acceptor) genetics
Phosphotransferases (Alcohol Group Acceptor) isolation & purification
Protein Binding drug effects
Protein Structure, Quaternary drug effects
Recombinant Proteins chemistry
Recombinant Proteins isolation & purification
Recombinant Proteins metabolism
Recombinant Proteins ultrastructure
Reducing Agents pharmacology
Solubility drug effects
Frataxin
Friedreich Ataxia metabolism
Iron pharmacology
Iron-Binding Proteins
Phosphotransferases (Alcohol Group Acceptor) metabolism
Saccharomyces cerevisiae cytology
Saccharomyces cerevisiae enzymology
Saccharomyces cerevisiae genetics
Subjects
Details
- Language :
- English
- ISSN :
- 0002-9297
- Volume :
- 67
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- American journal of human genetics
- Publication Type :
- Academic Journal
- Accession number :
- 10930361
- Full Text :
- https://doi.org/10.1086/303056