Electron tomography of ER, Golgi and related membrane systems

被引:44
作者
Donohoe, Bryon S. [1 ]
Mogelsvang, Soren [1 ]
Staehelin, L. Andrew [1 ]
机构
[1] Univ Colorado, Boulder, CO 80309 USA
关键词
cryofixation; electron microscopy; tomography; golgi; endoplasmic reticulum; membrane staining; three-dimensional;
D O I
10.1016/j.ymeth.2006.05.013
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A primary goal of cell biology is to uncover the mechanisms of cellular processes. A detailed structural understanding of the organelles and subcellular structures involved in these processes has often formed the foundation for the elucidation of their function. Electron tomography is a powerful technique for characterizing subcellular architecture and structural details in three dimensions. Electron tomography of cryofixed, freeze-substituted, and plastic-embedded samples allows three-dimensional visualization and display of dynamic, pleiomorphic structures at a resolution of similar to 7 nm in cell volumes up to similar to 25 mu m(3). In this review, we describe the electron tomography protocols that we have employed to determine the 3D architecture of complex cellular structures, thereby gaining insights into their functional organization. We stress the need for studying specimens preserved by cryolixation methods to obtain accurate information on the geometry and size of cellular structures. We also discuss some of the challenges associated with the staining of certain types of membranes. Finally, we provide examples of how tomographic data can be analyzed, dissected, and displayed using the tools built into the IMOD software package. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:154 / 162
页数:9
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