Literature DB >> 16480683

Characterization of the reaction products of cytochrome c with glutathione by mass spectrometry.

Haiteng Deng1.   

Abstract

Cytochrome c and glutathione (GSH) are two important biomolecules that regulate many cellular processes. The reaction of cytochrome c with GSH involves radical oxygen species and exhibits significant complexity. In the present work, the reaction of cytochrome c with GSH in water was characterized using mass spectrometry. The results show for the first time that the reaction generates multiple products including apocytochrome c in oxidized and reduced forms, glutathionylated apocytochrome c, GSH-modified cytochrome c, and oxidized and hydroxylated species. The reaction is O(2) dependent and is rapid in water at neutral pH and 37 degrees C. The reaction involves the cleavage of thioether linkages between the heme and apocytochrome c. Evidence for the role of H(2)O(2) and other oxygen radicals in this reaction is also provided.

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Year:  2006        PMID: 16480683     DOI: 10.1016/j.bbrc.2006.01.108

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  2 in total

1.  A novel role for cytochrome c: Efficient catalysis of S-nitrosothiol formation.

Authors:  Swati Basu; Agnes Keszler; Natalia A Azarova; Nneka Nwanze; Andreas Perlegas; Sruti Shiva; Katarzyna A Broniowska; Neil Hogg; Daniel B Kim-Shapiro
Journal:  Free Radic Biol Med       Date:  2009-10-29       Impact factor: 7.376

2.  The redox state of cytochrome c modulates resistance to methotrexate in human MCF7 breast cancer cells.

Authors:  Susana Barros; Núria Mencia; Laura Rodríguez; Carlota Oleaga; Conceição Santos; Verónique Noé; Carlos J Ciudad
Journal:  PLoS One       Date:  2013-05-13       Impact factor: 3.240

  2 in total

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