Macromolecular architecture in eukaryotic cells visualized by cryoelectron tomography

被引:606
作者
Medalia, O [1 ]
Weber, I [1 ]
Frangakis, AS [1 ]
Nicastro, D [1 ]
Gerisch, G [1 ]
Baumeister, W [1 ]
机构
[1] Max Planck Inst Biochem, D-82152 Martinsried, Germany
关键词
D O I
10.1126/science.1076184
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
Electron tomography of vitrifed cells is a noninvasive three-dimensional imaging technique that opens up new vistas for exploring the supramolecular organization of the cytoplasm. We applied this technique to Dictyostelium cells, focusing on the actin cytoskeleton. In actin networks reconstructed without prior removal of membranes or extraction of soluble proteins, the cross-linking of individual micro laments, their branching angles, and membrane attachment sites can be analyzed. At a resolution of 5 to 6 nanometers, single macromolecules with distinct shapes, such as the 26S proteasome, can be identified in an unperturbed cellular environment.
引用
收藏
页码:1209 / 1213
页数:5
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