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- W2963203485 abstract "The neurodegenerative disease Friedreich ataxia results from a deficiency of frataxin, a mitochondrial protein. Most patients have a GAA expansion in the first intron of both alleles of frataxin gene, whereas a minority of them are heterozygous for the expansion and contain a mutation in the other allele. Frataxin has been claimed to participate in iron homeostasis and biosynthesis of FeS clusters, however its role in both pathways is not unequivocally defined. In this work we combined different advanced spectroscopic analyses to explore the iron-binding properties of human frataxin, as isolated and at the FeS clusters assembly machinery. For the first time we used EPR spectroscopy to address this key issue providing clear evidence of the formation of a complex with a low symmetry coordination of the metal ion. By 2D NMR, we confirmed that iron can be bound in both oxidation states, a controversial issue, and, in addition, we were able to point out a transient interaction of frataxin with a N-terminal 6his-tagged variant of ISCU, the scaffold protein of the FeS clusters assembly machinery. To obtain insights on structure/function relationships relevant to understand the disease molecular mechanism(s), we extended our studies to four clinical frataxin mutants. All variants showed a moderate to strong impairment in their ability to activate the FeS cluster assembly machinery in vitro , while keeping the same iron-binding features of the wild type protein. This supports the multifunctional nature of frataxin and the complex biochemical consequences of its mutations. • Human frataxin binds iron in both oxidation states. • Small conformational changes of the ISCU flexible N terminus may help its interaction with frataxin. • Frataxin mutants with unaffected iron-binding are defective in FeS cluster assembly." @default.
- W2963203485 created "2019-07-30" @default.
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- W2963203485 date "2019-11-01" @default.
- W2963203485 modified "2023-10-09" @default.
- W2963203485 title "Exploring iron-binding to human frataxin and to selected Friedreich ataxia mutants by means of NMR and EPR spectroscopies" @default.
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- W2963203485 doi "https://doi.org/10.1016/j.bbapap.2019.07.007" @default.
- W2963203485 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/31344531" @default.
- W2963203485 hasPublicationYear "2019" @default.
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