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Campo DCValorIdioma
dc.contributor.authorRodrigues, Ana Paula-
dc.contributor.authorda Fonseca, Luiz Marcos-
dc.contributor.authorde Faria Oliveira, Olga M.-
dc.contributor.authorBrunetti, Iguatemy Lourenço-
dc.contributor.authorXimenes, Valdecir Farias-
dc.date.accessioned2014-05-20T13:24:26Z-
dc.date.accessioned2016-10-25T16:45:09Z-
dc.date.available2014-05-20T13:24:26Z-
dc.date.available2016-10-25T16:45:09Z-
dc.date.issued2006-12-01-
dc.identifierhttp://dx.doi.org/10.1016/j.bbagen.2006.09.008-
dc.identifier.citationBiochimica Et Biophysica Acta-general Subjects. Amsterdam: Elsevier B.V., v. 1760, n. 12, p. 1755-1761, 2006.-
dc.identifier.issn0304-4165-
dc.identifier.urihttp://hdl.handle.net/11449/7572-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/7572-
dc.description.abstractHorseradish peroxidase (HRP) is a plant enzyme widely used in biotechnology, including antibody-directed enzyme prodrug therapy (ADEPT). Here, we showed that HRP is able to catalyze the autoxidation of acetylacetone in the absence of hydrogen peroxide. This autoxidation led to generation of methylglyoxal and reactive oxygen species. The production of superoxide anion was evidenced by the effect of superoxide dismutase and by the generation of oxyperoxidase during the enzyme turnover. The HRP has a high specificity for acetylacetone, since the similar beta-dicarbonyls dimedon and acetoacetate were not oxidized. As this enzyme prodrug combination was highly cytotoxic for neutrophils and only requires the presence of a non-human peroxidase and acetylacetone, it might immediately be applied to research on the ADEPT techniques. The acetylacetone could be a starting point for the design of new drugs applied in HRP-related ADEPT techniques. (c) 2006 Elsevier B.V. All rights reserved.en
dc.format.extent1755-1761-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.subjecthorseradish peroxidasept
dc.subjectacetylacetonept
dc.subjectmethylglyoxalpt
dc.subjectreactive oxygen speciespt
dc.subjectantibody-directed enzyme prodrug therapypt
dc.titleOxidation of acetylacetone catalyzed by horseradish peroxidase in the absence of hydrogen peroxideen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationUNESP, Fac Ciências Farmaceut Araraquara, Dept Anal Clin, BR-14801902 Araraquara, SP, Brazil-
dc.description.affiliationUNESP, Inst Quim, Dept Biotecnol, BR-14801902 Araraquara, SP, Brazil-
dc.description.affiliationUniv Estadual Paulista, Fac Ciências, Dept Quim, Bauru, SP, Brazil-
dc.description.affiliationUnespUNESP, Fac Ciências Farmaceut Araraquara, Dept Anal Clin, BR-14801902 Araraquara, SP, Brazil-
dc.description.affiliationUnespUNESP, Inst Quim, Dept Biotecnol, BR-14801902 Araraquara, SP, Brazil-
dc.description.affiliationUnespUniv Estadual Paulista, Fac Ciências, Dept Quim, Bauru, SP, Brazil-
dc.identifier.doi10.1016/j.bbagen.2006.09.008-
dc.identifier.wosWOS:000242459500001-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofBiochimica et Biophysica Acta: General Subjects-
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