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Structural and molecular basis of the peroxynitrite-mediated nitration and inactivation of Trypanosoma cruzi iron-superoxide dismutases (Fe-SODs) A and B: disparate susceptibilities due to the repair of Tyr35 radical by Cys83 in Fe-SODB through intramolecular electron transfer
- Source :
- Journal of Biological Chemistry, Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2014, 289 (18), pp.12760-12778. ⟨10.1074/jbc.M113.545590⟩, CONICET Digital (CONICET), Consejo Nacional de Investigaciones Científicas y Técnicas, instacron:CONICET
- Publication Year :
- 2014
- Publisher :
- HAL CCSD, 2014.
-
Abstract
- Trypanosoma cruzi, the causative agent of Chagas disease, contains exclusively iron-dependent superoxide dismutases (Fe-SODs) located in different subcellular compartments. Peroxynitrite, a key cytotoxic and oxidizing effector biomolecule, reacted with T. cruzi mitochondrial (Fe-SODA) and cytosolic (Fe-SODB) SODs with second order rate constants of 4.6 ± 0.2 × 104 M−1 s−1 and 4.3 ± 0.4 × 104 M−1 s−1 at pH 7.4 and 37 °C, respectively. Both isoforms are dose-dependently nitrated and inactivated by peroxynitrite. Susceptibility of T. cruzi Fe-SODA toward peroxynitrite was similar to that reported previously for Escherichia coli Mn- and Fe-SODs and mammalian Mn-SOD, whereas Fe-SODB was exceptionally resistant to oxidant-mediated inactivation. We report mass spectrometry analysis indicating that peroxynitrite-mediated inactivation of T. cruzi Fe-SODs is due to the site-specific nitration of the critical and universally conserved Tyr35. Searching for structural differences, the crystal structure of Fe-SODA was solved at 2.2 Å resolution. Structural analysis comparing both Fe-SOD isoforms reveals differences in key cysteines and tryptophan residues. Thiol alkylation of Fe-SODB cysteines made the enzyme more susceptible to peroxynitrite. In particular, Cys83 mutation (C83S, absent in Fe-SODA) increased the Fe-SODB sensitivity toward peroxynitrite. Molecular dynamics, electron paramagnetic resonance, and immunospin trapping analysis revealed that Cys83 present in Fe-SODB acts as an electron donor that repairs Tyr35 radical via intramolecular electron transfer, preventing peroxynitrite-dependent nitration and consequent inactivation of Fe-SODB. Parasites exposed to exogenous or endogenous sources of peroxynitrite resulted in nitration and inactivation of Fe-SODA but not Fe-SODB, suggesting that these enzymes play distinctive biological roles during parasite infection of mammalian cells. Fil: Martinez, Alejandra. Universidad de la República; Uruguay Fil: Peluffo, Gonzalo. Universidad de la República; Uruguay Fil: Petruk, Ariel Alcides. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina. Universidad Nacional de Tucumán; Argentina Fil: Hugo, Martín. Universidad de la República; Uruguay Fil: Piñeyro, Dolores. Universidad de la República; Uruguay Fil: Demicheli, Veronica. Universidad de la República; Uruguay Fil: Moreno, Diego Martin. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Química Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario; Argentina Fil: Lima, Analia Ethel. Instituto Pasteur de Montevideo; Uruguay Fil: Batthyány, Carlos. Instituto Pasteur de Montevideo; Uruguay. Universidad de la República; Uruguay Fil: Duran, Rosario. Instituto Pasteur de Montevideo; Uruguay Fil: Robledo, Carlos Walter. Universidad de la República; Uruguay Fil: Marti, Marcelo Adrian. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina Fil: Larrieux, Nicole. Instituto Pasteur de Montevideo; Uruguay Fil: Buschiazzo, Alejandro. Instituto Pasteur de Montevideo; Uruguay. Instituto Pasteur; Francia Fil: Trujillo, Madia. Universidad de la República; Uruguay Fil: Radi, Rafael. Universidad de la República; Uruguay Fil: Piacenza, Lucia. Universidad de la República; Uruguay
- Subjects :
- Models, Molecular
Protozoan Proteins
MESH: Protein Structure, Secondary
MESH: Catalytic Domain
Crystallography, X-Ray
Protein Structure, Secondary
Peroxynitrite
MESH: Tyrosine
purl.org/becyt/ford/1 [https]
Catalytic Domain
MESH: Animals
MESH: Molecular Dynamics Simulation
MESH: Protozoan Proteins
MESH: Superoxide Dismutase
MESH: Peroxynitrous Acid
Trypanosoma Cruzi
MESH: Kinetics
Superoxide
MESH: Reactive Oxygen Species
Molecular Bases of Disease
[SDV.BBM.BC]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Biomolecules [q-bio.BM]
Isoenzymes
MESH: Mutagenesis, Site-Directed
MESH: Nitrates
MESH: Isoenzymes
Oxidation-Reduction
MESH: Trypanosoma cruzi
CIENCIAS NATURALES Y EXACTAS
Superoxide Dismutase (Sod)
Superoxide Dismutase (SOD)
MESH: Models, Molecular
Protein Binding
MESH: Enzyme Activation
Nitration
Free Radicals
Otras Ciencias Biológicas
Trypanosoma cruzi
Blotting, Western
Molecular Dynamics Simulation
Nitric Oxide
Trypanosome
MESH: Host-Parasite Interactions
Host-Parasite Interactions
Ciencias Biológicas
Electron Transport
Peroxynitrous Acid
[CHIM.CRIS]Chemical Sciences/Cristallography
Animals
MESH: Blotting, Western
MESH: Protein Binding
Chagas Disease
MESH: Chagas Disease
[SDV.BBM]Life Sciences [q-bio]/Biochemistry, Molecular Biology
Cysteine
purl.org/becyt/ford/1.6 [https]
MESH: Electron Transport
Binding Sites
Nitrates
Superoxide Dismutase
Electron Spin Resonance Spectroscopy
MESH: Cysteine
MESH: Crystallography, X-Ray
Enzyme Activation
Kinetics
MESH: Binding Sites
Mutagenesis, Site-Directed
Tyrosine
MESH: Electron Spin Resonance Spectroscopy
Reactive Oxygen Species
Subjects
Details
- Language :
- English
- ISSN :
- 00219258 and 1083351X
- Database :
- OpenAIRE
- Journal :
- Journal of Biological Chemistry, Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2014, 289 (18), pp.12760-12778. ⟨10.1074/jbc.M113.545590⟩, CONICET Digital (CONICET), Consejo Nacional de Investigaciones Científicas y Técnicas, instacron:CONICET
- Accession number :
- edsair.pmid.dedup....2cf2014f1f37e1f2fed6eb09383930d5
- Full Text :
- https://doi.org/10.1074/jbc.M113.545590⟩