Proteasome-dependent degradation of oxidized proteins in MRC-5 fibroblasts

被引:152
作者
Sitte, N
Merker, K
Grune, T
机构
[1] Humboldt Univ, Fac Med Charite, Clin Phys Med, D-10098 Berlin, Germany
[2] Humboldt Univ, Fac Med Charite, Clin Rehabil, D-10098 Berlin, Germany
关键词
protein oxidation; fibroblast; proteasome; lactacystin;
D O I
10.1016/S0014-5793(98)01495-1
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
Fibroblasts were exposed to various concentrations of hydrogen peroxide and the removal of oxidized proteins was followed by determining protein-bound carbonyls, Fibroblasts are able to increase the turnover of metabolically radiolabeled proteins after treatment with hydrogen peroxide, It was demonstrated for the first time, that the increased protein turnover was accompanied by a removal of protein-bound carbonyl groups. The proteasome-specific inhibitor lactacystin was able to inhibit the elimination of protein-bound carbonyl groups. Therefore, the key role of the proteasome in the degradation of oxidized proteins in fibroblasts could be demonstrated, (C) 1998 Federation of European Biochemical Societies.
引用
收藏
页码:399 / 402
页数:4
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