Acetyl Radical Production by the Methylglyoxal-Peroxynitrite System: A Possible Route for L-Lysine Acetylation


Autoria(s): MASSARI, Julio; TOKIKAWA, Rita; ZANOLLI, Luiz; TAVARES, Marina Franco Maggi; ASSUNCAO, Nilson Antonio; BECHARA, Etelvino Jose Henriques
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2010

Resumo

Methylglyoxal is an a-oxoaldehyde putatively produced in excess from triose phosphates, aminoacetone, and acetone in some disorders, particularly in diabetes. Here, we investigate the nucleophilic addition of ONOO(-), known as a potent oxidant and nucleophile, to methylglyoxal, yielding an acetyl radical intermediate and ultimately formate and acetate ions. The rate of ONOO(-) decay in the presence of methylglyoxal [k(2,app) = (1.0 +/- 0.1) x 10(3) M(-1) s(-1); k(2) approximate to 1.0 x 10(5) M(-1) s(-1)] at pH 7.2 and 25 degrees C was found to be faster than that reported with monocarbonyl substrates (k(2) < 10(3) M(-1) diacetyl (k(2) = 1.0 x 10(4) M(-1) s(-1)), or CO(2) (k(2) = 3-6 x 10(4) M(-1) s(-1)). The pH profile of the methylglyoxal peroxynitrite reaction describes an ascendant curve with an inflection around pH 7.2, which roughly coincides with the pK(a) values of both ONOOH and H(2)PO(4)(-) ion. Electron paramagnetic resonance spin trapping experiments with 2-methyl-2-nitrosopropane revealed concentration-dependent formation of an adduct that can be attributed to 2-methyl-2-nitrosopropane-CH(3)CO(center dot) (a(N) = 0.83 mT). Spin trapping with 3,5-dibromo-4-nitrosobenzene sulfonate gave a signal that could be assigned to a methyl radical adduct [a(N) = 1.41 mT; a(H) = 1.35 mT; a(H(m)) = 0.08 mT]. The 2-methyl-2-nitrosopropane-CH(3)CO(center dot) adduct could also be observed by replacement of ONOO(-) with H(2)O(2), although at much lower yields. Acetyl radicals could be also trapped by added L-lysine as indicated by the presence of W-acetyl-L-lysine in the spent reaction mixture. This raises the hypothesis that ONOO(-)/H(2)O(2) in the presence of methylglyoxal is endowed with the potential to acetylate proteins in post-translational processes.

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 Cientifico e Tecnologico (CNPq)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Instituto Nacional de Ciencia e Tecnologia (INCT) Redoxoma

Instituto Nacional de Ciencia e Tecnologia (INCT) Redoxoma

Identificador

CHEMICAL RESEARCH IN TOXICOLOGY, v.23, n.11, p.1762-1770, 2010

0893-228X

http://producao.usp.br/handle/BDPI/30957

10.1021/tx1002244

http://dx.doi.org/10.1021/tx1002244

Idioma(s)

eng

Publicador

AMER CHEMICAL SOC

Relação

Chemical Research in Toxicology

Direitos

restrictedAccess

Copyright AMER CHEMICAL SOC

Palavras-Chave #TANDEM MASS-SPECTROMETRY #SPIN-TRAP #CARBON-DIOXIDE #NITRIC-OXIDE #BIOLOGICAL-ACTIVITY #LIVING ORGANISMS #KINETICS #DECOMPOSITION #OXIDATION #NITRATION #Chemistry, Medicinal #Chemistry, Multidisciplinary #Toxicology
Tipo

article

original article

publishedVersion