Interaction of frataxin, an iron binding protein, with IscU of Fe-S clusters biogenesis pathway and its upregulation in AmpB resistant Leishmania donovani

Biochimie. 2015 Aug:115:120-35. doi: 10.1016/j.biochi.2015.05.016. Epub 2015 May 30.

Abstract

Leishmania donovani is a unicellular protozoon parasite that causes visceral leishmaniasis (VL), which is a fatal disease if left untreated. Certain Fe-S proteins of the TCA cycle and respiratory chain have been found in the Leishmania parasite but the precise mechanisms for their biogenesis and the maturation of Fe-S clusters remains unknown. Fe-S clusters are ubiquitous cofactors of proteins that perform critical cellular functions. The clusters are biosynthesized by the mitochondrial Iron-Sulphur Cluster (ISC) machinery with core protein components that include the catalytic cysteine desulphurase IscS, the scaffold proteins IscU and IscA, and frataxin as an iron carrier/donor. However, no information regarding frataxin, its regulation, or its role in drug resistance is available for the Leishmania parasite. In this study, we characterized Ld-frataxin to investigate its role in the ISC machinery of L. donovani. We expressed and purified the recombinant Ld-frataxin protein and observed its interaction with Ld-IscU by co-purification and pull-down assay. Furthermore, we observed that the cysteine desulphurase activity of the purified Ld-IscS protein was stimulated in the presence of Ld-frataxin and Ld-IscU, particularly in the presence of iron; neither Ld-frataxin nor Ld-IscU alone had significant effects on Ld-IscS activity. Interestingly, RT-PCR and western blotting showed that Ld-frataxin is upregulated in AmpB-resistant isolates compared to sensitive strains, which may support higher Fe-S protein activity in AmpB-resistant L. donovani. Additionally, Ld-frataxin was localized in the mitochondria, as revealed by digitonin fractionation and indirect immunofluorescence. Thus, our results suggest the role of Ld-frataxin as an iron binding/carrier protein for Fe-S cluster biogenesis that physically interacts with other core components of the ISC machinery within the mitochondria.

Keywords: Frataxin; ISC machinery; Ld-frataxin; Leishmania donovani; Protein–protein interaction; [Fe–S] clusters.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Amphotericin B / pharmacology*
  • Animals
  • Binding Sites
  • Carbon-Sulfur Lyases / metabolism
  • Cloning, Molecular
  • Drug Resistance*
  • Female
  • Frataxin
  • Humans
  • Iron / metabolism
  • Iron-Binding Proteins / chemistry
  • Iron-Binding Proteins / genetics
  • Iron-Binding Proteins / isolation & purification
  • Iron-Binding Proteins / metabolism*
  • Iron-Sulfur Proteins / biosynthesis*
  • Iron-Sulfur Proteins / metabolism*
  • Leishmania donovani / drug effects
  • Leishmania donovani / metabolism*
  • Mice
  • Models, Molecular
  • Molecular Sequence Data
  • Phylogeny
  • Protein Binding
  • Protein Conformation
  • Protein Transport
  • Protozoan Proteins / chemistry
  • Protozoan Proteins / genetics
  • Protozoan Proteins / isolation & purification
  • Protozoan Proteins / metabolism
  • Sequence Analysis
  • Up-Regulation*

Substances

  • Iron-Binding Proteins
  • Iron-Sulfur Proteins
  • Protozoan Proteins
  • Amphotericin B
  • Iron
  • Carbon-Sulfur Lyases
  • cysteine desulfurase