Stiffened lipid platforms at molecular force foci

被引:68
作者
Anishkin, Andriy [1 ,2 ]
Kung, Ching [3 ]
机构
[1] Penn State Univ, Dept Biochem, Huck Inst Life Sci, University Pk, PA 16802 USA
[2] Penn State Univ, Ctr Computat Prote, Huck Inst Life Sci, University Pk, PA 16802 USA
[3] Univ Wisconsin, Dept Genet, Lab Cell & Mol Biol, Madison, WI 53706 USA
基金
美国国家卫生研究院;
关键词
force sensing; lipid bilayer; lipid rafts; mechanosensitivity; TOUCH RECEPTOR NEURONS; CELL-CELL CONTACTS; MECHANOSENSITIVE CHANNELS; ESCHERICHIA-COLI; CRYSTAL-STRUCTURE; POTASSIUM CHANNELS; MEMBRANE DOMAINS; ION CHANNELS; PROTEIN; STOMATIN;
D O I
10.1073/pnas.1302018110
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
How mechanical forces are sensed remains largely mysterious. The forces that gate prokaryotic and several eukaryotic channels were found to come from the lipid membrane. Our survey of animal cells found that membrane force foci all have cholesterol-gathering proteins and are reinforced with cholesterol. This result is evident in overt force sensors at the tips of stereocilia for vertebrate hearing and the touch receptor of Caenorhabditis elegans and mammalian neurons. For less specialized cells, cadherins sustain the force between neighboring cells and integrins between cells and matrix. These tension bearers also pass through and bind to a cholesterol-enriched platform before anchoring to cytoskeleton through other proteins. Cholesterol, in alliance with sphingomyelin and specialized proteins, enforces a more ordered structure in the bilayer. Such a stiffened platform can suppress mechanical noise, redirect, rescale, and confine force. We speculate that such platforms may be dynamic. The applied force may allow disordered-phase lipids to enter the platform-staging channel opening in the thinner mobile neighborhood. The platform may also contain specialized protein/lipid subdomains enclosing mechanosensitive channels to open with localized tension. Such a dynamic stage can mechanically operate structurally disparate channels or enzymes without having to tie them directly to cadherin, integrin, or other protein tethers.
引用
收藏
页码:4886 / 4892
页数:7
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