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
Link To Document :
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