Tyrosinase-catalyzed binding of 3,4-dihydroxyphenylalanine with proteins through the sulfhydryl group

Biochim Biophys Acta. 1986 May 2;881(3):415-21. doi: 10.1016/0304-4165(86)90034-6.

Abstract

The cytotoxicity of catechols has been ascribed to covalent binding of the omicron-quinone oxidation products to proteins through sulfhydryl groups. The nature of the covalent binding was studied with dopaquinone formed on tyrosinase oxidation of 3,4-dihydroxyphenylalanine (DOPA). After acid hydrolysis of the reaction products, cysteinyldopas liberated (protein-bound cysteinyldopas) were determined by HPLC with electrochemical detection. When 0.1 mM DOPA was oxidized in the presence of 0.2 mM bovine serum albumin, alcohol dehydrogenase or isocitrate dehydrogenase, protein-bound cysteinyldopas were formed in yields of 5.4, 44, or 33%, respectively. The covalent binding was almost completely inhibited by 1 mM cysteine or 1 mM ascorbic acid, but 10 mM lysine had no effect. These results unambiguously demonstrate that dopaquinone can bind with proteins mostly through sulfhydryl groups.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alcohol Dehydrogenase
  • Alcohol Oxidoreductases / metabolism
  • Basidiomycota / enzymology
  • Binding Sites
  • Catechol Oxidase / metabolism*
  • Cysteine
  • Dihydroxyphenylalanine / metabolism*
  • Isocitrate Dehydrogenase / metabolism
  • Monophenol Monooxygenase / metabolism*
  • Protein Binding
  • Saccharomyces cerevisiae / enzymology
  • Sulfhydryl Compounds

Substances

  • Sulfhydryl Compounds
  • Dihydroxyphenylalanine
  • Alcohol Oxidoreductases
  • Alcohol Dehydrogenase
  • Isocitrate Dehydrogenase
  • Catechol Oxidase
  • Monophenol Monooxygenase
  • Cysteine