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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

Authors :
Martinez, Alejandra
Peluffo, Gonzalo
Petruk, Ariel
Hugo, Martín
Piñeyro, Dolores
Demicheli, Verónica
Moreno, Diego M
Lima, Analía
Batthyany, Carlos
Durán, Rosario
Robello, Carlos
Marti, Marcelo
Larrieux, Nicole
Buschiazzo, Alejandro
Trujillo, Madia
Radi, Rafael
Piacenza, Lucía
Universidad de la República [Montevideo] (UCUR)
Universidad de Buenos Aires [Buenos Aires] (UBA)
Molecular Biology / Biología Molecular [Montevideo]
Institut Pasteur de Montevideo
Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)
Universidad Nacional de Rosario [Santa Fe]
Analytical Biochemistry and Proteomics / Bioquímica y Proteómica Analíticas [Montevideo]
Protein Crystallography / Cristalografía de Proteínas [Montevideo]
his work was supported, in whole or in part, by National Institutes of Health Grant 1R01AI095173. This work was also supported by a grant from the Universidad de la República (CSIC, Uruguay) (to R. R.) and by PEDECIBA (Progama de Desarrollo de Ciencias Básicas, Uruguay) and CeBEM (Centro de Biología Estructural del Mercosur).
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

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

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⟩