Production and quenching of reactive oxygen species by pterin derivatives, an intriguing class of biomolecules

Autores
Oliveros, Esther; Dántola, María Laura; Vignoni, Mariana; Thomas, Andrés Héctor; Lorente, Carolina
Año de publicación
2011
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Pterins, a family of heterocyclic compounds derived from 2-aminopteridin-4(1H)-one, are widespread in living systems and participate in important biological functions, such as metabolic redox processes. Under UV-A excitation (320-400 nm), aromatic pterins (Pt) can generate reactive oxygen species (ROS), as a consequence of both energy-and electron-transfer processes from their triplet excited state. Quantum yields of singlet oxygen (1O2) production depend largely on the nature of the substituents on the pterin moiety and on the pH. Formation of the superoxide anion by electron transfer between the pterin radical anion and molecular oxygen leads to the production of significant amounts of hydrogen peroxide (H2O2) by disproportionation. Dihydropterins (H2Pt) do not produce 1O2 but are oxidized by this species with high rate constants yielding pterins as well as H2O2. In contrast to aromatic derivatives, H2Pt are oxidized by H2O2, and rates and products strongly depend on the nature of the substituents on the H2Pt moiety. Aromatic pterins have been found in vivo under pathological conditions, e.g., biopterin or 6-carboxypterin are present in the skin of patients affected by vitiligo, a depigmentation disorder. The biomedical implications of the production of ROS by pterin derivatives and their reactivity with these species are discussed.
Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas
Materia
Química
Hydrogen peroxide
Photochemical reactivity
Pterin derivatives
Quantum yields
Rate constants
Reactive oxygen species (ros)
Singlet oxygen
Superoxide anion
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by-nc-sa/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/83980

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network_name_str SEDICI (UNLP)
spelling Production and quenching of reactive oxygen species by pterin derivatives, an intriguing class of biomoleculesOliveros, EstherDántola, María LauraVignoni, MarianaThomas, Andrés HéctorLorente, CarolinaQuímicaHydrogen peroxidePhotochemical reactivityPterin derivativesQuantum yieldsRate constantsReactive oxygen species (ros)Singlet oxygenSuperoxide anionPterins, a family of heterocyclic compounds derived from 2-aminopteridin-4(1H)-one, are widespread in living systems and participate in important biological functions, such as metabolic redox processes. Under UV-A excitation (320-400 nm), aromatic pterins (Pt) can generate reactive oxygen species (ROS), as a consequence of both energy-and electron-transfer processes from their triplet excited state. Quantum yields of singlet oxygen (1O2) production depend largely on the nature of the substituents on the pterin moiety and on the pH. Formation of the superoxide anion by electron transfer between the pterin radical anion and molecular oxygen leads to the production of significant amounts of hydrogen peroxide (H2O2) by disproportionation. Dihydropterins (H2Pt) do not produce 1O2 but are oxidized by this species with high rate constants yielding pterins as well as H2O2. In contrast to aromatic derivatives, H2Pt are oxidized by H2O2, and rates and products strongly depend on the nature of the substituents on the H2Pt moiety. Aromatic pterins have been found in vivo under pathological conditions, e.g., biopterin or 6-carboxypterin are present in the skin of patients affected by vitiligo, a depigmentation disorder. The biomedical implications of the production of ROS by pterin derivatives and their reactivity with these species are discussed.Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas2011info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf801-811http://sedici.unlp.edu.ar/handle/10915/83980enginfo:eu-repo/semantics/altIdentifier/issn/0033-4545info:eu-repo/semantics/altIdentifier/doi/10.1351/PAC-CON-10-08-22info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/4.0/Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-10-15T11:08:02Zoai:sedici.unlp.edu.ar:10915/83980Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-10-15 11:08:02.89SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv Production and quenching of reactive oxygen species by pterin derivatives, an intriguing class of biomolecules
title Production and quenching of reactive oxygen species by pterin derivatives, an intriguing class of biomolecules
spellingShingle Production and quenching of reactive oxygen species by pterin derivatives, an intriguing class of biomolecules
Oliveros, Esther
Química
Hydrogen peroxide
Photochemical reactivity
Pterin derivatives
Quantum yields
Rate constants
Reactive oxygen species (ros)
Singlet oxygen
Superoxide anion
title_short Production and quenching of reactive oxygen species by pterin derivatives, an intriguing class of biomolecules
title_full Production and quenching of reactive oxygen species by pterin derivatives, an intriguing class of biomolecules
title_fullStr Production and quenching of reactive oxygen species by pterin derivatives, an intriguing class of biomolecules
title_full_unstemmed Production and quenching of reactive oxygen species by pterin derivatives, an intriguing class of biomolecules
title_sort Production and quenching of reactive oxygen species by pterin derivatives, an intriguing class of biomolecules
dc.creator.none.fl_str_mv Oliveros, Esther
Dántola, María Laura
Vignoni, Mariana
Thomas, Andrés Héctor
Lorente, Carolina
author Oliveros, Esther
author_facet Oliveros, Esther
Dántola, María Laura
Vignoni, Mariana
Thomas, Andrés Héctor
Lorente, Carolina
author_role author
author2 Dántola, María Laura
Vignoni, Mariana
Thomas, Andrés Héctor
Lorente, Carolina
author2_role author
author
author
author
dc.subject.none.fl_str_mv Química
Hydrogen peroxide
Photochemical reactivity
Pterin derivatives
Quantum yields
Rate constants
Reactive oxygen species (ros)
Singlet oxygen
Superoxide anion
topic Química
Hydrogen peroxide
Photochemical reactivity
Pterin derivatives
Quantum yields
Rate constants
Reactive oxygen species (ros)
Singlet oxygen
Superoxide anion
dc.description.none.fl_txt_mv Pterins, a family of heterocyclic compounds derived from 2-aminopteridin-4(1H)-one, are widespread in living systems and participate in important biological functions, such as metabolic redox processes. Under UV-A excitation (320-400 nm), aromatic pterins (Pt) can generate reactive oxygen species (ROS), as a consequence of both energy-and electron-transfer processes from their triplet excited state. Quantum yields of singlet oxygen (1O2) production depend largely on the nature of the substituents on the pterin moiety and on the pH. Formation of the superoxide anion by electron transfer between the pterin radical anion and molecular oxygen leads to the production of significant amounts of hydrogen peroxide (H2O2) by disproportionation. Dihydropterins (H2Pt) do not produce 1O2 but are oxidized by this species with high rate constants yielding pterins as well as H2O2. In contrast to aromatic derivatives, H2Pt are oxidized by H2O2, and rates and products strongly depend on the nature of the substituents on the H2Pt moiety. Aromatic pterins have been found in vivo under pathological conditions, e.g., biopterin or 6-carboxypterin are present in the skin of patients affected by vitiligo, a depigmentation disorder. The biomedical implications of the production of ROS by pterin derivatives and their reactivity with these species are discussed.
Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas
description Pterins, a family of heterocyclic compounds derived from 2-aminopteridin-4(1H)-one, are widespread in living systems and participate in important biological functions, such as metabolic redox processes. Under UV-A excitation (320-400 nm), aromatic pterins (Pt) can generate reactive oxygen species (ROS), as a consequence of both energy-and electron-transfer processes from their triplet excited state. Quantum yields of singlet oxygen (1O2) production depend largely on the nature of the substituents on the pterin moiety and on the pH. Formation of the superoxide anion by electron transfer between the pterin radical anion and molecular oxygen leads to the production of significant amounts of hydrogen peroxide (H2O2) by disproportionation. Dihydropterins (H2Pt) do not produce 1O2 but are oxidized by this species with high rate constants yielding pterins as well as H2O2. In contrast to aromatic derivatives, H2Pt are oxidized by H2O2, and rates and products strongly depend on the nature of the substituents on the H2Pt moiety. Aromatic pterins have been found in vivo under pathological conditions, e.g., biopterin or 6-carboxypterin are present in the skin of patients affected by vitiligo, a depigmentation disorder. The biomedical implications of the production of ROS by pterin derivatives and their reactivity with these species are discussed.
publishDate 2011
dc.date.none.fl_str_mv 2011
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Articulo
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://sedici.unlp.edu.ar/handle/10915/83980
url http://sedici.unlp.edu.ar/handle/10915/83980
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/issn/0033-4545
info:eu-repo/semantics/altIdentifier/doi/10.1351/PAC-CON-10-08-22
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by-nc-sa/4.0/
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc-sa/4.0/
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
dc.format.none.fl_str_mv application/pdf
801-811
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instname:Universidad Nacional de La Plata
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repository.name.fl_str_mv SEDICI (UNLP) - Universidad Nacional de La Plata
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