3-Hydroxykynurenine and 3-hydroxyanthranilic acid generate hydrogen peroxide and promote α-crystallin cross-linking by metal ion reduction

被引:173
作者
Goldstein, LE
Leopold, MC
Huang, XD
Atwood, CS
Saunders, AJ
Hartshorn, M
Lim, JT
Faget, KY
Muffat, JA
Scarpa, RC
Chylack, LT
Bowden, EF
Tanzi, RE
Bush, AI
机构
[1] Massachusetts Gen Hosp, Lab Oxidat Biol, Dept Psychiat, Charlestown, MA 02129 USA
[2] Massachusetts Gen Hosp, Dept Neurol, Genet Aging Unit, Charlestown, MA 02129 USA
[3] Brigham & Womens Hosp, Ctr Ophthalm Res, Boston, MA 02115 USA
[4] N Carolina State Univ, Dept Chem, Raleigh, NC 27695 USA
关键词
D O I
10.1021/bi992997s
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The kynurenine pathway catabolite 3-hydroxykynurenine (3HK) and redox-active metals such as copper and iron are implicated in cataractogenesis, Here we investigate the reaction of kynurenine pathway catabolites with copper and iron, as well as interactions with the major lenticular structural proteins, the alpha-crystallins. The o-aminophenol kynurenine catabolites 3HK and 3-hydroxyanthranilic acid (3HAA) reduced Cu(II)>Fe(III) to Cu(I) and Fe(II), respectively, whereas quinolinic acid and the nonphenolic kynurenine catabolites kynurenine and anthranilic acid did not reduce either metal. Both 3HK and 3HAA generated superoxide and hydrogen peroxide in a copper-dependent manner. In addition, 3HK and 3HAA fostered copper-dependent alpha-crystallin cross-linking. 3HK- or 3HAA-modifed alpha-crystallin showed enhanced redox activity in comparison to unmodified alpha-crystallin or ascorbate-modified alpha-crystallin. These data support the possibility that 3HK and 3HAA may be cofactors in the oxidative damage of proteins, such as alpha-crystallin, through interactions with redox-active metals and especially copper. These findings may have relevance for understanding cataractogenesis and other degenerative conditions in which the kynurenine pathway is activated.
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页码:7266 / 7275
页数:10
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