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Novel Protein Modification by Kynurenine in Human Lenses
It is known that human lenses increase in color and fluorescence with age, but the molecular basis for this is not well understood. We demonstrate here that proteins isolated from human lenses contain significant levels of the UV filter kynurenine covalently bound to histidine and lysine residues. I...
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Published in: | The Journal of biological chemistry 2002-02, Vol.277 (7), p.4867-4873 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | It is known that human lenses increase in color and fluorescence with age, but the molecular basis for this is not well understood.
We demonstrate here that proteins isolated from human lenses contain significant levels of the UV filter kynurenine covalently
bound to histidine and lysine residues. Identification was confirmed by synthesis of the kynurenine amino acid adducts and
comparison of the chromatographic retention times and mass spectra of these authentic standards with those of corresponding
adducts isolated from human lenses following acid hydrolysis. Using calf lens proteins as a model, covalent binding of kynurenine
to lens proteins has been shown to proceed via side chain deamination in a manner analogous to that observed for the related
UV filter, 3-hydroxykynurenine O- β- d -glucoside. Levels of histidylkynurenine and lysylkynurenine were low in human lenses in subjects younger than 30, but thereafter
increased in concentration with the age of the individual. Post-translational modification of lens proteins by tryptophan
metabolites therefore appears to be responsible, at least in part, for the age-dependent increase in coloration and fluorescence
of the human lens, and this process may also be important in other tissues in which up-regulation of tryptophan catabolism
occurs. |
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ISSN: | 0021-9258 1083-351X |
DOI: | 10.1074/jbc.M107529200 |