Photosensitized electron transfer within a self-assembled norharmane–2′-deoxyadenosine 5′-monophosphate (dAMP) complex
- Autores
- Gonzalez, M. Micaela; Rasse Suriani, Federico Ariel Osvaldo; Franca, Carlos Alberto; Pis Diez, Reinaldo; Gholipour, Yousef; Nonami, Hiroshi; Erra-Balsells, Rosa; Cabrerizo, Franco Martín
- Año de publicación
- 2012
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Norharmane is a compound that belongs to a family of alkaloids called β-carbolines (βCs). These alkaloids are present in a wide range of biological systems, playing a variety of significant photo-dependent roles. Upon UV-A irradiation, βCs are able to act as efficient photosensitizers. In this work, we have investigated the photosensitized oxidation of 2′-deoxyadenosine 5′-monophosphate (dAMP) by norharmane in an aqueous phase, upon UV-A (350 nm) irradiation. The effect of the pH was evaluated on both the interactions between norharmane and dAMP in the ground and electronic excited states, and on the dAMP photosensitized oxidation. A quite strong static interaction between norharmane and dAMP was observed, especially under those pH conditions where the protonated form of the alkaloid is present (pH < 7). Theoretical studies were performed to further characterize the static complex structure. The participation of reactive oxygen species (ROS) in the photosensitized reaction was also investigated and the photoproducts were characterized by means of UV-LDI-MS and ESI-MS. All the data provided herein indicate that electron transfer (Type I) within a self-assembled norharmane–dAMP complex is the operative mechanism in the dAMP photosensitization.
Centro de Química Inorgánica - Materia
-
Química
Bioquímica
norharmane
alkaloids
photosensitized oxidation
dAMP - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by/3.0/
- Repositorio
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/151505
Ver los metadatos del registro completo
id |
SEDICI_0a6bcc705c51aa6593f1ecf741c7c7aa |
---|---|
oai_identifier_str |
oai:sedici.unlp.edu.ar:10915/151505 |
network_acronym_str |
SEDICI |
repository_id_str |
1329 |
network_name_str |
SEDICI (UNLP) |
spelling |
Photosensitized electron transfer within a self-assembled norharmane–2′-deoxyadenosine 5′-monophosphate (dAMP) complexGonzalez, M. MicaelaRasse Suriani, Federico Ariel OsvaldoFranca, Carlos AlbertoPis Diez, ReinaldoGholipour, YousefNonami, HiroshiErra-Balsells, RosaCabrerizo, Franco MartínQuímicaBioquímicanorharmanealkaloidsphotosensitized oxidationdAMPNorharmane is a compound that belongs to a family of alkaloids called β-carbolines (βCs). These alkaloids are present in a wide range of biological systems, playing a variety of significant photo-dependent roles. Upon UV-A irradiation, βCs are able to act as efficient photosensitizers. In this work, we have investigated the photosensitized oxidation of 2′-deoxyadenosine 5′-monophosphate (dAMP) by norharmane in an aqueous phase, upon UV-A (350 nm) irradiation. The effect of the pH was evaluated on both the interactions between norharmane and dAMP in the ground and electronic excited states, and on the dAMP photosensitized oxidation. A quite strong static interaction between norharmane and dAMP was observed, especially under those pH conditions where the protonated form of the alkaloid is present (pH < 7). Theoretical studies were performed to further characterize the static complex structure. The participation of reactive oxygen species (ROS) in the photosensitized reaction was also investigated and the photoproducts were characterized by means of UV-LDI-MS and ESI-MS. All the data provided herein indicate that electron transfer (Type I) within a self-assembled norharmane–dAMP complex is the operative mechanism in the dAMP photosensitization.Centro de Química Inorgánica2012-11info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf9359-9372http://sedici.unlp.edu.ar/handle/10915/151505enginfo:eu-repo/semantics/altIdentifier/issn/1477-0520info:eu-repo/semantics/altIdentifier/issn/1477-0539info:eu-repo/semantics/altIdentifier/doi/10.1039/C2OB26462Einfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/3.0/Creative Commons Attribution 3.0 Unported (CC BY 3.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-03T11:11:04Zoai:sedici.unlp.edu.ar:10915/151505Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-03 11:11:04.887SEDICI (UNLP) - Universidad Nacional de La Platafalse |
dc.title.none.fl_str_mv |
Photosensitized electron transfer within a self-assembled norharmane–2′-deoxyadenosine 5′-monophosphate (dAMP) complex |
title |
Photosensitized electron transfer within a self-assembled norharmane–2′-deoxyadenosine 5′-monophosphate (dAMP) complex |
spellingShingle |
Photosensitized electron transfer within a self-assembled norharmane–2′-deoxyadenosine 5′-monophosphate (dAMP) complex Gonzalez, M. Micaela Química Bioquímica norharmane alkaloids photosensitized oxidation dAMP |
title_short |
Photosensitized electron transfer within a self-assembled norharmane–2′-deoxyadenosine 5′-monophosphate (dAMP) complex |
title_full |
Photosensitized electron transfer within a self-assembled norharmane–2′-deoxyadenosine 5′-monophosphate (dAMP) complex |
title_fullStr |
Photosensitized electron transfer within a self-assembled norharmane–2′-deoxyadenosine 5′-monophosphate (dAMP) complex |
title_full_unstemmed |
Photosensitized electron transfer within a self-assembled norharmane–2′-deoxyadenosine 5′-monophosphate (dAMP) complex |
title_sort |
Photosensitized electron transfer within a self-assembled norharmane–2′-deoxyadenosine 5′-monophosphate (dAMP) complex |
dc.creator.none.fl_str_mv |
Gonzalez, M. Micaela Rasse Suriani, Federico Ariel Osvaldo Franca, Carlos Alberto Pis Diez, Reinaldo Gholipour, Yousef Nonami, Hiroshi Erra-Balsells, Rosa Cabrerizo, Franco Martín |
author |
Gonzalez, M. Micaela |
author_facet |
Gonzalez, M. Micaela Rasse Suriani, Federico Ariel Osvaldo Franca, Carlos Alberto Pis Diez, Reinaldo Gholipour, Yousef Nonami, Hiroshi Erra-Balsells, Rosa Cabrerizo, Franco Martín |
author_role |
author |
author2 |
Rasse Suriani, Federico Ariel Osvaldo Franca, Carlos Alberto Pis Diez, Reinaldo Gholipour, Yousef Nonami, Hiroshi Erra-Balsells, Rosa Cabrerizo, Franco Martín |
author2_role |
author author author author author author author |
dc.subject.none.fl_str_mv |
Química Bioquímica norharmane alkaloids photosensitized oxidation dAMP |
topic |
Química Bioquímica norharmane alkaloids photosensitized oxidation dAMP |
dc.description.none.fl_txt_mv |
Norharmane is a compound that belongs to a family of alkaloids called β-carbolines (βCs). These alkaloids are present in a wide range of biological systems, playing a variety of significant photo-dependent roles. Upon UV-A irradiation, βCs are able to act as efficient photosensitizers. In this work, we have investigated the photosensitized oxidation of 2′-deoxyadenosine 5′-monophosphate (dAMP) by norharmane in an aqueous phase, upon UV-A (350 nm) irradiation. The effect of the pH was evaluated on both the interactions between norharmane and dAMP in the ground and electronic excited states, and on the dAMP photosensitized oxidation. A quite strong static interaction between norharmane and dAMP was observed, especially under those pH conditions where the protonated form of the alkaloid is present (pH < 7). Theoretical studies were performed to further characterize the static complex structure. The participation of reactive oxygen species (ROS) in the photosensitized reaction was also investigated and the photoproducts were characterized by means of UV-LDI-MS and ESI-MS. All the data provided herein indicate that electron transfer (Type I) within a self-assembled norharmane–dAMP complex is the operative mechanism in the dAMP photosensitization. Centro de Química Inorgánica |
description |
Norharmane is a compound that belongs to a family of alkaloids called β-carbolines (βCs). These alkaloids are present in a wide range of biological systems, playing a variety of significant photo-dependent roles. Upon UV-A irradiation, βCs are able to act as efficient photosensitizers. In this work, we have investigated the photosensitized oxidation of 2′-deoxyadenosine 5′-monophosphate (dAMP) by norharmane in an aqueous phase, upon UV-A (350 nm) irradiation. The effect of the pH was evaluated on both the interactions between norharmane and dAMP in the ground and electronic excited states, and on the dAMP photosensitized oxidation. A quite strong static interaction between norharmane and dAMP was observed, especially under those pH conditions where the protonated form of the alkaloid is present (pH < 7). Theoretical studies were performed to further characterize the static complex structure. The participation of reactive oxygen species (ROS) in the photosensitized reaction was also investigated and the photoproducts were characterized by means of UV-LDI-MS and ESI-MS. All the data provided herein indicate that electron transfer (Type I) within a self-assembled norharmane–dAMP complex is the operative mechanism in the dAMP photosensitization. |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012-11 |
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/10915/151505 |
url |
http://sedici.unlp.edu.ar/handle/10915/151505 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/issn/1477-0520 info:eu-repo/semantics/altIdentifier/issn/1477-0539 info:eu-repo/semantics/altIdentifier/doi/10.1039/C2OB26462E |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/3.0/ Creative Commons Attribution 3.0 Unported (CC BY 3.0) |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://creativecommons.org/licenses/by/3.0/ Creative Commons Attribution 3.0 Unported (CC BY 3.0) |
dc.format.none.fl_str_mv |
application/pdf 9359-9372 |
dc.source.none.fl_str_mv |
reponame:SEDICI (UNLP) instname:Universidad Nacional de La Plata instacron:UNLP |
reponame_str |
SEDICI (UNLP) |
collection |
SEDICI (UNLP) |
instname_str |
Universidad Nacional de La Plata |
instacron_str |
UNLP |
institution |
UNLP |
repository.name.fl_str_mv |
SEDICI (UNLP) - Universidad Nacional de La Plata |
repository.mail.fl_str_mv |
alira@sedici.unlp.edu.ar |
_version_ |
1842260614578176000 |
score |
13.13397 |