Electron microscopy of integrins

被引:10
作者
Adair, Brian D. [1 ]
Yeager, Mark
机构
[1] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 92037 USA
[2] Scripps Clin, Div Cardiovasc Dis, La Jolla, CA USA
来源
INTEGRINS | 2007年 / 426卷
关键词
D O I
10.1016/S0076-6879(07)26015-X
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Integrins are a family of heterodimeric, cell-surface receptors that mediate interactions between the cytoskeleton and the extracellular matrix. We have used electron microscopy and single-particle image analysis combined with molecular modeling to investigate the structures of the full-length integrin alpha(11b)beta(3) and the ectodomain of alpha(V)beta(3) in a complex with fibronectin. The full-length integrin alpha(11b)beta(3) is purified from human platelets by ion exchange and get filtration chromatography in buffers containing the detergent octyl-beta-D-glucopyranoside, whereas the recombinant ectodomain of alpha(V)beta(3) is soluble in aqueous buffer. Transmission electron microscopy is performed either in negative stain, where the protein is embedded in a heavy metal such as uranyl acetate, or in the frozen-hydrated state, where the sample is flash-frozen such that the buffer is vitrified and native conditions are preserved. Individual integrin particles are selected from low-dose micrographs, either by manual identification or an automated method using a cross-correlation search of the micrograph against
引用
收藏
页码:337 / +
页数:38
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