Vinculin forms a directionally asymmetric catch bond with F-actin

被引:197
作者
Huang, Derek L. [1 ]
Bax, Nicolas A. [2 ]
Buckley, Craig D. [3 ]
Weis, William I. [1 ,2 ,4 ]
Dunn, Alexander R. [1 ,3 ,5 ]
机构
[1] Stanford Univ, Biophys Program, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Struct Biol, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Mol & Cellular Physiol, Stanford, CA 94305 USA
[5] Stanford Univ, Stanford Cardiovasc Inst, Stanford, CA 94305 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
DEPENDENT MANNER; CELL-ADHESION; FORCE; MIGRATION; FILAMENTS; POLARITY; BINDING; LAMELLIPODIA; ORGANIZATION; MECHANISMS;
D O I
10.1126/science.aan2556
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
Vinculin is an actin-binding protein thought to reinforce cell-cell and cell-matrix adhesions. However, how mechanical load affects the vinculin-F-actin bond is unclear. Using a single-molecule optical trap assay, we found that vinculin forms a force-dependent catch bond with F-actin through its tail domain, but with lifetimes that depend strongly on the direction of the applied force. Force toward the pointed (-) end of the actin filament resulted in a bond that was maximally stable at 8 piconewtons, with a mean lifetime (12 seconds) 10 times as long as the mean lifetime when force was applied toward the barbed (+) end. A computational model of lamellipodial actin dynamics suggests that the directionality of the vinculin-F-actin bond could establish long-range order in the actin cytoskeleton. The directional and force-stabilized binding of vinculin to F-actin may be a mechanism by which adhesion complexes maintain front-rear asymmetry in migrating cells.
引用
收藏
页码:703 / 706
页数:4
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