dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T13:24:26Z
dc.date.accessioned2022-10-05T13:13:38Z
dc.date.available2014-05-20T13:24:26Z
dc.date.available2022-10-05T13:13:38Z
dc.date.created2014-05-20T13:24:26Z
dc.date.issued2006-12-01
dc.identifierBiochimica Et Biophysica Acta-general Subjects. Amsterdam: Elsevier B.V., v. 1760, n. 12, p. 1755-1761, 2006.
dc.identifier0304-4165
dc.identifierhttp://hdl.handle.net/11449/7572
dc.identifier10.1016/j.bbagen.2006.09.008
dc.identifierWOS:000242459500001
dc.identifier4066413997908572
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3884413
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.
dc.languageeng
dc.publisherElsevier B.V.
dc.relationBiochimica et Biophysica Acta: General Subjects
dc.relation3.679
dc.relation1,671
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.subjecthorseradish peroxidase
dc.subjectacetylacetone
dc.subjectmethylglyoxal
dc.subjectreactive oxygen species
dc.subjectantibody-directed enzyme prodrug therapy
dc.titleOxidation of acetylacetone catalyzed by horseradish peroxidase in the absence of hydrogen peroxide
dc.typeArtigo


Este ítem pertenece a la siguiente institución