Stretching Single Talin Rod Molecules Activates Vinculin Binding

被引:1127
作者
del Rio, Armando [1 ]
Perez-Jimenez, Raul [1 ]
Liu, Ruchuan [2 ]
Roca-Cusachs, Pere [1 ]
Fernandez, Julio M. [1 ]
Sheetz, Michael P. [1 ]
机构
[1] Columbia Univ, Dept Biol Sci, New York, NY 10027 USA
[2] Natl Univ Singapore, Dept Phys, Singapore 117542, Singapore
关键词
FORCE; PROTEIN; SITES; STABILITY; UBIQUITIN; COMPLEX; BUNDLE;
D O I
10.1126/science.1162912
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The molecular mechanism by which a mechanical stimulus is translated into a chemical response in biological systems is still unclear. We show that mechanical stretching of single cytoplasmic proteins can activate binding of other molecules. We used magnetic tweezers, total internal reflection fluorescence, and atomic force microscopy to investigate the effect of force on the interaction between talin, a protein that links liganded membrane integrins to the cytoskeleton, and vinculin, a focal adhesion protein that is activated by talin binding, leading to reorganization of the cytoskeleton. Application of physiologically relevant forces caused stretching of single talin rods that exposed cryptic binding sites for vinculin. Thus in the talin- vinculin system, molecular mechanotransduction can occur by protein binding after exposure of buried binding sites in the talin-vinculin system. Such protein stretching may be a more general mechanism for force transduction.
引用
收藏
页码:638 / 641
页数:4
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