Detection of lipid-lysine amide-type adduct as a marker of PUFA oxidation and its applications
Research into lipid peroxidation-induced protein modification has been ongoing for many years. Recent studies on lipo-oxidation shows the occurrence of another type of protein modification, amide-type adduct formation by lipid hydroperoxide, as well as classical aldehyde-derived protein modification...
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Published in | Archives of biochemistry and biophysics Vol. 501; no. 2; pp. 182 - 187 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
15.09.2010
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Subjects | |
Online Access | Get full text |
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Summary: | Research into lipid peroxidation-induced protein modification has been ongoing for many years. Recent studies on lipo-oxidation shows the occurrence of another type of protein modification, amide-type adduct formation by lipid hydroperoxide, as well as classical aldehyde-derived protein modifications. The amide-type modifications can be either classified as alkylamide and carboxyalkylamide according to the formed structures. As an alkylamide-type adduct, Nε-(hexanoyl)lysine can be formed by the reaction of peroxidized
n
−
6 fatty acid with lysine. Nε-(propanoyl)lysine is considered to be generated from oxidation of
n
−
3 fatty acid with lysine. The generation pattern of both might be useful for classification of which fatty acids are more involved in oxidation
in vivo. Since the alkylamide type-adducts are relatively stable and detectable from biological specimens like urine, these adducts, especially Nε-(hexanoyl)lysine, are used as reliable markers for not only oxidative stress evaluation but also development of functional food. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 |
ISSN: | 0003-9861 1096-0384 |
DOI: | 10.1016/j.abb.2010.06.010 |