Cytochrome c-promoted cardiolipin oxidation generates singlet molecular oxygen


Autoria(s): Miyamoto, Sayuri; Nantes, Iseli L.; Faria, Priscila A.; Cunha, Daniela; Ronsein, Graziella E.; Medeiros, Marisa Helena Gennari de; Mascio, Paolo Di
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

29/10/2013

29/10/2013

2012

Resumo

The interaction of cytochrome c (cyt c) with cardiolipin (CL) induces protein conformational changes that favor peroxidase activity. This process has been correlated with CL oxidation and the induction of cell death. Here we report evidence demonstrating the generation of singlet molecular oxygen [O-2((1)Delta(g))] by a cyt c-CL complex in a model membrane containing CL. The formation of singlet oxygen was directly evidenced by luminescence measurements at 1270 nm and by chemical trapping experiments. Singlet oxygen generation required cyt c-CL binding and occurred at pH values higher than 6, consistent with lipid-protein interactions involving fully deprotonated CL species and positively charged residues in the protein. Moreover, singlet oxygen formation was specifically observed for tetralinoleoyl CL species and was not observed with monounsaturated and saturated CL species. Our results show that there are at least two mechanisms leading to singlet oxygen formation: one with fast kinetics involving the generation of singlet oxygen directly from CL hydroperoxide decomposition and the other involving CL oxidation. The contribution of the first mechanism was clearly evidenced by the detection of labeled singlet oxygen [O-18(2)((1)Delta(g))] from liposomes supplemented with 18-oxygen-labeled CL hydroperoxides. However quantitative analysis showed that singlet oxygen yield from CL hydroperoxides was minor (<5%) and that most of the singlet oxygen is formed from the second mechanism. Based on these data and previous findings we propose a mechanism of singlet oxygen generation through reactions involving peroxyl radicals (Russell mechanism) and excited triplet carbonyl intermediates (energy transfer mechanism).

FAPESP (Fundacao de Amparo a Pesquisa do Estado de Sao Paulo)

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Conselho Nacional para o Desenvolvimento Cientifico e Tecnologico (CNPq)

CNPq (Conselho Nacional para o Desenvolvimento Cientifico e Tecnologico)

CAPES/PROCAD-NF (Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior/Programa Nacional de Cooperacao Academica Novas Fronteiras)

CAPES/PROCADNF (Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior/Programa Nacional de Cooperacao Academica Novas Fronteiras)

INCT de Processos Redox em Biomedicina - Redoxoma

INCT de Processos Redox em Biomedicina Redoxoma

NAPRedoxoma

NAP-Redoxoma

L'OREAL-UNESCO for Women in Science

LOREALUNESCO for Women in Science

John Simon Guggenheim Memorial Foundation

John Simon Memorial Guggenheim Foundation

Identificador

PHOTOCHEMICAL & PHOTOBIOLOGICAL SCIENCES, CAMBRIDGE, v. 11, n. 10, pp. 1536-1546, OCT, 2012

1474-905X

http://www.producao.usp.br/handle/BDPI/36322

10.1039/c2pp25119a

http://dx.doi.org/10.1039/c2pp25119a

Idioma(s)

eng

Publicador

ROYAL SOC CHEMISTRY

CAMBRIDGE

Relação

PHOTOCHEMICAL & PHOTOBIOLOGICAL SCIENCES

Direitos

openAccess

Copyright ROYAL SOC CHEMISTRY

Palavras-Chave #LINOLEIC-ACID HYDROPEROXIDE #PHOTODYNAMIC THERAPY #LIPID-PEROXIDATION #HYDROGEN-PEROXIDE #FREE-RADICALS #HEME IRON #MITOCHONDRIA #APOPTOSIS #MEMBRANES #RELEASE #BIOCHEMISTRY & MOLECULAR BIOLOGY #BIOPHYSICS #CHEMISTRY, PHYSICAL
Tipo

article

original article

publishedVersion