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Investigating the Antioxidant Properties of Oxo-Sulfur Compounds on Metal-Mediated DNA Damage
Main Group Chem (2007)
  • Ria R. Ramoutar, Georgia Southern University
  • Julia L. Brumaghim, Clemson University
Abstract

The organosulfur compounds allicin, methionine and methylcysteine protect against metal-mediated oxidative DNA damage, but few studies have determined the antioxidant behaviour of the oxo-sulfur derivatives of these compounds. Gel electrophoresis experiments were performed to determine the ability of MetSO, MeCysSO, MMTS, MePhSO and Me2SO2 to inhibit copper- and iron-mediated DNA damage. Under these conditions, MetSO and MeCysSO significantly inhibit DNA damage, MePhSO and Me2SO2 have no effect and MMTS promotes DNA damage. For iron-mediated DNA damage, significantly less antioxidant or pro-oxidant behaviour is observed for these compounds. To determine whether metal coordination is a mechanism for the antioxidant activity of these oxo-sulfur compounds, UV–vis spectroscopy and gel electrophoresis experiments using [Cu(bipy)2]+ or [Fe(EDTA)]2− as the metal source were also performed. Results of these experiments indicate that metal coordination is a significant factor for their antioxidant activity, but another mechanism also contributes to their antioxidant behaviour.

Keywords
  • DNA Damage Inhibition,
  • Antioxidant,
  • Oxo-Sulfur Compounds
Disciplines
Publication Date
2007
Citation Information
Ria R. Ramoutar and Julia L. Brumaghim. "Investigating the Antioxidant Properties of Oxo-Sulfur Compounds on Metal-Mediated DNA Damage" Main Group Chem Vol. 6 (2007)
Available at: http://works.bepress.com/ria_ramoutar/6/