• Title of article

    Oxidation of methionyl residues in proteins: Tools, targets, and reversal

  • Author/Authors

    Walther Vogt، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 1995
  • Pages
    13
  • From page
    93
  • To page
    105
  • Abstract
    Methionine (Met) is one of the most readily oxidized amino acid constituents of proteins. It is attacked by H2O2, hydroxyl radicals, hypochlorite, chloramines, and peroxynitrite, all these oxidants being produced in biological systems. The oxidation product, Met sulfoxide, can be reduced back to Met by Met sulfoxide reductase. Numerous proteins lose functional activity by Met oxidation. However, functional activation of proteins by Met oxidation has also been observed. Functional changes by Met oxidation in a given protein appear to have pathophysiological significance in some cases. Considering the reversibility of Met oxidation and the functional changes associated with the oxidation, it seems possible that Met oxidation/ reduction in proteins may be one means to control homeostasis in biologicals systems.
  • Keywords
    Methionine oxidation , Methionine sulfoxide reduction , protein , Activation/inactivation by Met oxidation , free radicals
  • Journal title
    Free Radical Biology and Medicine
  • Serial Year
    1995
  • Journal title
    Free Radical Biology and Medicine
  • Record number

    517013