Abstract
Cellular oxidative stress promotes chemical reactions causing damage to DNA, proteins, and membranes. Here, we describe experiments indicating that reactive oxygen species, in addition to degrading polypeptides and polynucleotides through direct reactions, can also promote damaging biomolecular cross reactivity by converting protein residues into peroxides that cleave the DNA backbone. The studies reported show that a variety of residues induce strand scission upon oxidation, and hydrogen abstraction occurring at the DNA backbone is responsible for the damage. The observation of peptide-promoted DNA damage suggests that crossreations within protein/DNA complexes should be considered as a significant cause of the toxicity of reactive oxygen species.
Original language | English (US) |
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Pages (from-to) | 695-701 |
Number of pages | 7 |
Journal | Chemistry and Biology |
Volume | 12 |
Issue number | 6 |
DOIs | |
State | Published - 2005 |
Externally published | Yes |
Funding
We would like to acknowledge financial support from the National Science Foundation (CAREER award to S.O.K.) and the Sloan Research Foundation (Research Fellowship to S.O.K.).
ASJC Scopus subject areas
- Drug Discovery
- Molecular Medicine
- Molecular Biology
- Biochemistry
- Clinical Biochemistry
- Pharmacology