Molecular gymnastics: serpin structure, folding and misfolding

被引:113
作者
Whisstock, James C. [1 ]
Bottomley, Stephen P. [1 ]
机构
[1] Dept Biochem & Mol Biol, Prot Crystallog Unit, Melbourne, Vic 3800, Australia
基金
澳大利亚研究理事会; 英国医学研究理事会;
关键词
D O I
10.1016/j.sbi.2006.10.005
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
The native state of serpins represents a long-lived intermediate or metastable structure on the serpin folding pathway. Upon interaction with a protease, the serpin trap is sprung and the molecule continues to fold into a more stable conformation. However, thermodynamic stability can also be achieved through alternative, unproductive folding pathways that result in the formation of inactive conformations. Our increasing understanding of the mechanism of protease inhibition and the dynamics of native serpin structures has begun to reveal how evolution has harnessed the actual process of protein folding (rather than the final folded outcome) to elegantly achieve function. The cost of using metastability for function, however, is an increased propensity for misfolding.
引用
收藏
页码:761 / 768
页数:8
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