Protein folding, misfolding, and aggregation. formation of inclusion bodies and aggresomes

被引:124
作者
Markossian, KA [1 ]
Kurganov, BI [1 ]
机构
[1] Russian Acad Sci, Bach Inst Biochem, Moscow 119071, Russia
基金
俄罗斯基础研究基金会;
关键词
folding; misfolding; aggregation; inclusion bodies; aggresomes; chaperones; proteasomes; microtubules;
D O I
10.1023/B:BIRY.0000043539.07961.4c
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
In this review the mechanisms of protein folding, misfolding, and aggregation as well as the mechanisms of cell defense against toxic protein aggregates are considered. Misfolded and aggregated proteins in cells are exposed to chaperone-mediated refolding and are degraded by proteasomes if refolding is impossible. Proteolysis-stable protein aggregates accumulate, forming inclusion bodies. In eucaryotic cells, protein aggregates form structures in the pericentrosomal area that have been termed "aggresomes". Formation of aggresomes in cells is a general cellular response to the presence of misfolded proteins when the degrading capacity of the cells is exceeded. The role of aggresomes in disturbance of the proteasomal system operation and in cellular death, particularly in the so-called "protein conformational diseases", is discussed.
引用
收藏
页码:971 / 984
页数:14
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