Calcium and magnesium ions modulate the oligomeric state and function of mitochondrial 2-Cys peroxiredoxins in Leishmania parasites

J Biol Chem. 2017 Apr 28;292(17):7023-7039. doi: 10.1074/jbc.M116.762039. Epub 2017 Mar 14.

Abstract

Leishmania parasites have evolved a number of strategies to cope with the harsh environmental changes during mammalian infection. One of these mechanisms involves the functional gain that allows mitochondrial 2-Cys peroxiredoxins to act as molecular chaperones when forming decamers. This function is critical for parasite infectivity in mammals, and its activation has been considered to be controlled exclusively by the enzyme redox state under physiological conditions. Herein, we have revealed that magnesium and calcium ions play a major role in modulating the ability of these enzymes to act as molecular chaperones, surpassing the redox effect. These ions are directly involved in mitochondrial metabolism and participate in a novel mechanism to stabilize the decameric form of 2-Cys peroxiredoxins in Leishmania mitochondria. Moreover, we have demonstrated that a constitutively dimeric Prx1m mutant impairs the survival of Leishmania under heat stress, supporting the central role of the chaperone function of Prx1m for Leishmania parasites during the transition from insect to mammalian hosts.

Keywords: Leishmania; calcium; molecular chaperone; oligomerization; peroxiredoxin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anisotropy
  • Calcium / metabolism*
  • Chromatography
  • Disulfides / chemistry
  • Fluorometry
  • Gene Expression Regulation
  • Homeodomain Proteins / metabolism
  • Humans
  • Hydrogen-Ion Concentration
  • Leishmania / metabolism*
  • Light
  • Magnesium / metabolism*
  • Mitochondria / metabolism
  • Mitochondrial Proteins / metabolism*
  • Molecular Chaperones / metabolism
  • Mutagenesis, Site-Directed
  • Oxidation-Reduction
  • Oxygen / chemistry
  • Peroxiredoxins / metabolism*
  • Protein Multimerization
  • Protozoan Proteins / metabolism*
  • Scattering, Radiation
  • Temperature

Substances

  • Disulfides
  • Homeodomain Proteins
  • Mitochondrial Proteins
  • Molecular Chaperones
  • PRRX2 protein, human
  • Protozoan Proteins
  • 2-cys peroxiredoxin, human
  • Peroxiredoxins
  • Magnesium
  • Oxygen
  • Calcium

Associated data

  • PDB/4KB3
  • PDB/4KCE
  • PDB/4LLR
  • PDB/1QMV