3D structure determination of native mammalian cells using cryo-FIB and cryo-electron tomography

被引:60
|
作者
Wang, Ke [1 ]
Strunk, Korrinn [2 ]
Zhao, Gongpu [1 ]
Gray, Jennifer L. [2 ]
Zhang, Peijun [1 ]
机构
[1] Univ Pittsburgh, Sch Med, Dept Biol Struct, Pittsburgh, PA 15260 USA
[2] Univ Pittsburgh, Sch Engn, Dept Mech Engn & Mat Sci, Pittsburgh, PA 15260 USA
基金
美国国家卫生研究院;
关键词
Cryo-ET; Cryo-FIB; Lamella; HeLa cell; Mitochondria; E; coli; Membranes; Nuclear pore; ELECTRON TOMOGRAPHY; MOLECULAR ARCHITECTURE; DIRECT VISUALIZATION; VITREOUS SECTIONS; IN-SITU; EUKARYOTIC CELLS; LIGHT-MICROSCOPY; RECEPTOR ARRAYS; VIRUS; TISSUE;
D O I
10.1016/j.jsb.2012.07.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cryo-electron tomography (cryo-ET) has enabled high resolution three-dimensional(3D) structural analysis of virus and host cell interactions and many cell signaling events; these studies, however, have largely been limited to very thin, peripheral regions of eukaryotic cells or to small prokaryotic cells. Recent efforts to make thin, vitreous sections using cryo-ultramicrotomy have been successful, however,this method is technically very challenging and with many artifacts. Here, we report a simple and robust method for creating in situ, frozen-hydrated cell lamellas using a focused ion beam at cryogenic temperature (cryo-FIB), allowing access to any interior cellular regions of interest. We demonstrate the utility of cryo-FIB with high resolution 3D cellular structures from both bacterial cells and large mammalian cells. The method will not only facilitate high-throughput 3D structural analysis of biological specimens, but is also broadly applicable to sample preparation of thin films and surface materials without the need for FIB "lift-out". (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:318 / 326
页数:9
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