Journal
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Volume 297, Issue 2, Pages 206-213Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/S0006-291X(02)02143-5
Keywords
apolipoproteinA-I; apolipoproteinA-I-Milano; apolipoproteinA-I-Paris; amphipathic alpha helix; synthetic peptides; antioxidant activity; reactive oxygen species; superoxide anions; lipid peroxidation; oxidized phospholipid
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Funding
- NHLBI NIH HHS [HL59483, HL55493] Funding Source: Medline
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Apolipoprotein(apo)A-I-Milano (R173C) and apoA-I-Paris (R151C) are rare cysteine variants of wild-type (WT) apoA-I that possess novel antioxidant properties on phospholipid surfaces. Yet, the two variants differ in their ability to inhibit lipid peroxidation. In this study, we used synthetic peptides (18 mers) to investigate the structural basis for the difference in antioxidant activity between apoA-I-Milano and apoA-I-Paris. A peptide (aa 167-R173C-184) based on the amphipathic a helix harboring the R173C mutation inhibited superoxide anion-mediated oxidation of phospholipid in a dose-dependent manner, but it failed to directly quench superoxide anions in aqueous solution, indicating that the peptide acted at the level of phospholipid to inhibit lipid peroxidation just like the full-length cysteine variant. Peptide 145-R151C-162 based on the helical segment containing R 15 1 C exhibited the same capacity as peptide 167-R173C-184 to inhibit lipid peroxidation. Thus, the difference in antioxidant activity between apoA-I-Milano and apoA-I-Paris was not governed by the primary amino acid sequence of their individual amphipathic a helices, rather contextual constraints within the full-length variants set the difference in antioxidant activity. Cysteine-free peptides were weak inhibitors of lipid peroxidation. These results suggest that thiol-bearing helical peptides based on apoA-I-Milano may be useful to combat inflammatory related diseases. (C) 2002 Elsevier Science (USA). All rights reserved.
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