Histidine and Proline are Important Sites of Free Radical Damage to Proteins
- 1 January 1989
- journal article
- Published by Taylor & Francis in Free Radical Research Communications
- Vol. 7 (2) , 97-103
- https://doi.org/10.3109/10715768909087929
Abstract
Our hypothesis that proline and histidine are major sites of damage during radical attack upon proteins, becoming respectively glutamate and aspartate, was investigated using proteins biosynthetically labelled with radioactive proline or histidine as targets. Free radicals were generated by copper and H2O2, or by gamma radiolysis. Protein-bound histidine was substantially converted into aspartate. Much proline was modified during radical attack, but it was not converted into glutamate. We conclude that histidine and proline are important sites of protein attack by radicals; protein cleavage may result from these reactions.Keywords
This publication has 19 references indexed in Scilit:
- Is enhanced free radical flux associated with increased intracellular proteolysis?FEBS Letters, 1987
- Fragmentation of proteins by free radicals and its effect on their susceptibility to enzymic hydrolysisBiochemical Journal, 1986
- Intracellular proteolytic systems may function as secondary antioxidant defenses: An hypothesisJournal of Free Radicals in Biology & Medicine, 1986
- Free radicals, lipids and protein degradationTrends in Biochemical Sciences, 1986
- Studies of the limited degradation of mucus glycoproteins. The mechanism of the peroxide reactionBiochemical Journal, 1985
- Endogenous free radical generation may influence proteolysis in MitochondriaBiochemical and Biophysical Research Communications, 1985
- Intracellular protein degradation in cultures of dystrophic muscle cells and fibroblastsExperimental Cell Research, 1984
- Oxygen Effect in the Radiolysis of ProteinsInternational Journal of Radiation Biology, 1984
- A Method for Quantitative Amino Acid Analysis Using Precolumn o-Phthalaldehyde Derivatization and High Performance Liquid ChromatographyJournal of Chromatographic Science, 1981
- Reverse-phase liquid chromatographic analysis of amino acids after reaction with o-phthalaldehydeAnalytical Biochemistry, 1980