Characterization of iron-sulfur protein assembly in isolated mitochondria. A requirement for ATP, NADH, and reduced iron

J Biol Chem. 2002 Aug 16;277(33):29810-6. doi: 10.1074/jbc.M204675200. Epub 2002 Jun 13.

Abstract

To study the biochemical requirements for maturation of iron-sulfur (Fe/S) proteins, we have reconstituted the process in vitro using detergent extracts from Saccharomyces cerevisiae mitochondria. Efficient assembly of biotin synthase as a model Fe/S protein required anaerobic conditions, dithiothreitol, cysteine, ATP, and NADH. Cysteine is utilized by the cysteine desulfurase Nfs1p to release sulfan sulfur; ATP presumably reflects the function of the Hsp70 family chaperone Ssq1p; and NADH is used for reduction of the ferredoxin Yah1p involved in Fe/S protein biogenesis. Hence, our assay system faithfully reproduces the in vivo pathway. We have further investigated the involvement of various mitochondrial proteins suspected to participate in Fe/S protein biogenesis. In mitochondrial extracts depleted in Isa1p, Fe/S protein formation was severely decreased. A similar strong decline was observed with extracts from Delta yfh1 mitochondria, indicating that both Isa1p and the yeast frataxin homologue, Yfh1p, are crucial for biogenesis of mitochondrial Fe/S proteins. Conversely, the activities of mitochondrial extracts from Delta nfu1 cells were only moderately reduced, suggesting a dispensable role for Nfu1p. Finally, iron utilized for Fe/S protein formation was imported into the matrix of intact mitochondria in ferrous form in a membrane potential-dependent transport step. Our results represent the first in vitro reconstitution of the entire pathway of Fe/S protein maturation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism*
  • Carrier Proteins / metabolism
  • Detergents
  • Frataxin
  • Iron / metabolism*
  • Iron-Binding Proteins*
  • Iron-Sulfur Proteins / metabolism*
  • Membrane Potentials
  • Mitochondria / metabolism*
  • NAD / metabolism*
  • Oxidation-Reduction
  • Saccharomyces cerevisiae / metabolism

Substances

  • Carrier Proteins
  • Detergents
  • Iron-Binding Proteins
  • Iron-Sulfur Proteins
  • NAD
  • Adenosine Triphosphate
  • Iron