Unfolding forces of titin and fibronectin domains directly measured by AFM

被引:0
作者
Rief, M [1 ]
Gautel, M
Gaub, HE
机构
[1] Stanford Univ, Sch Med, Stanford, CA 94305 USA
[2] EMBL, Biol Struct Div, Heidelberg, Germany
[3] Univ Munich, Munich, Germany
来源
ELASTIC FILAMENTS OF THE CELL | 2000年 / 481卷
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暂无
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
AFM-based Single Molecule Force Spectroscopy provides a new tool for probing the mechanical properties of single molecules. In this chapter we show that the unfolding forces of single protein domains can be directly measured. Unfolding forces give new insight into protein stability that cannot be deduced from thermodynamic measurements. A comparison between the unfolding forces measured in Ig domains of the muscle protein titin and those measured in fibronectin Type III domains reveals an extraordinarily high stability of titin domains.
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页码:129 / 141
页数:13
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