Peroxymonocarbonate and Carbonate Radical Displace the Hydroxyl-like Oxidant in the Sod1 Peroxidase Activity under Physiological Conditions


Autoria(s): MEDINAS, Danilo B.; TOLEDO JR., Jose C.; CERCHIARO, Giselle; DO-AMARAL, Antonia T.; DE-REZENDE, Leandro; MALVEZZI, Alberto; AUGUSTO, Ohara
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2009

Resumo

Despite being one of the most important antioxidant defenses, Cu,Zn-superoxide dismutase (Sod1) has been frequently associated with harmful effects, including neurotoxicity. This toxicity has been attributed to immature forms of Sod1 and extraneous catalytic activities. Among these, the ability of Sod1 to function as a peroxidase may be particularly relevant because it is increased in bicarbonate buffer and produces the reactive carbonate radical. Despite many studies, how this radical forms remains unknown. To address this question, we systematically studied hSod1 peroxidase activity in the presence of nitrite, formate, and bicarbonate-carbon dioxide. Kinetic analyses of hydrogen peroxide consumption and of nitrite, formate, and bicarbonate-carbon dioxide oxidation showed that the Sod1-bound hydroxyl-like oxidant functions in the presence of nitrite and formate. In the presence of bicarbonate-carbon dioxide, this oxidant is replaced by peroxymonocarbonate, which is then reduced to the carbonate radical. Peroxymonocarbonate intermediacy was evidenced by (13)C NMR experiments showing line broadening of its peak in the presence of Zn,ZnSod1. In agreement, peroxymonocarbonate was docked into the hSod1 active site, where it interacted with the conserved Arg(143). Also, a reaction between peroxymonocarbonate and Cu(I)Sod1 was demonstrated by stopped-flow experiments. Kinetic simulations indicated that peroxymonocarbonate is produced during Sod1 turnover and not in bulk solution. In the presence of bicarbonate-carbon dioxide, sustained hSod1-mediated oxidations occurred with low steady-state concentrations of hydrogen peroxide (4-10 mu M). Thus, carbonate radical formation through peroxymonocarbonate may be a key event in Sod1-induced toxicity.

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

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Conselho Nacional de Desenvolvimento Cientifico a Tecnologico (CNPq)

Identificador

CHEMICAL RESEARCH IN TOXICOLOGY, v.22, n.4, p.639-648, 2009

0893-228X

http://producao.usp.br/handle/BDPI/30842

10.1021/tx800287m

http://dx.doi.org/10.1021/tx800287m

Idioma(s)

eng

Publicador

AMER CHEMICAL SOC

Relação

Chemical Research in Toxicology

Direitos

restrictedAccess

Copyright AMER CHEMICAL SOC

Palavras-Chave #ZINC SUPEROXIDE-DISMUTASE #AMYOTROPHIC-LATERAL-SCLEROSIS #CU,ZN-SUPEROXIDE DISMUTASE #HYDROGEN-PEROXIDE #COVALENT AGGREGATION #OXIDATION-PRODUCTS #NITROGEN-DIOXIDE #BICARBONATE #COPPER #ANION #Chemistry, Medicinal #Chemistry, Multidisciplinary #Toxicology
Tipo

article

original article

publishedVersion