Demethylation of methionine and keratin damage in human hair

被引:12
作者
Borowczyk, Kamila [1 ,2 ]
Suliburska, Joanna [3 ]
Jakubowski, Hieronim [1 ,4 ]
机构
[1] Rutgers New Jersey Med Sch, Dept Microbiol Biochem & Mol Genet, Int Ctr Publ Hlth, 225 Warren St, Newark, NJ 07103 USA
[2] Univ Lodz, Dept Environm Chem, PL-90236 Lodz, Poland
[3] Poznan Univ Life Sci, Dept Human Nutr & Hyg, PL-60632 Poznan, Poland
[4] Poznan Univ Life Sci, Dept Biochem & Biotechnol, PL-60632 Poznan, Poland
关键词
Hair keratin damage; Homocysteine; Methionine demethylation; Copper; Iron; PROTEIN N-HOMOCYSTEINYLATION; QUALITY-CONTROL; HUMAN PLASMA; AMINO-ACIDS; THIOLACTONE; MECHANISM; OXIDATION; RESIDUES; MICE;
D O I
10.1007/s00726-018-2545-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Growing human head hair contains a history of keratin and provides a unique model for studies of protein damage. Here, we examined mechanism of homocysteine (Hcy) accumulation and keratin damage in human hair. We found that the content of Hcy-keratin increased along the hair fiber, with levels 5-10-fold higher levels in older sections at the hair's tip than in younger sections at hair's base. The accumulation of Hcy led to a complete loss of keratin solubility in sodium dodecyl sulfate. The increase in Hcy-keratin was accompanied by a decrease in methionine-keratin. Levels of Hcy-keratin were correlated with hair copper and iron in older hair. These relationships were recapitulated in model experiments in vitro, in which Hcy generation from Met exhibited a similar dependence on copper or iron. Taken together, these findings suggest that Hcy-keratin accumulation is due to copper/iron-catalyzed demethylation of methionine residues and contributes to keratin damage in human hair.
引用
收藏
页码:537 / 546
页数:10
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