Multi-resolution correlative focused ion beam scanning electron microscopy: Applications to cell biology

被引:69
作者
Narayan, Kedar [1 ]
Danielson, Cindy M. [2 ]
Lagarec, Ken [3 ]
Lowekamp, Bradley C. [4 ]
Coffman, Phil [1 ]
Laquerre, Alexandre [3 ]
Phaneuf, Michael W. [3 ]
Hope, Thomas J. [2 ]
Subramaniam, Sriram [1 ]
机构
[1] NCI, Cell Biol Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
[2] Northwestern Univ, Dept Cell & Mol Biol, Chicago, IL 60611 USA
[3] Fibics Inc, Ottawa, ON K1A 0G1, Canada
[4] NIH, Natl Lib Med, Bethesda, MD 20892 USA
关键词
Three-dimensional electron microscopy; Ion abrasion scanning electron microscopy; Correlative microscopy; HIV-1; core; 3D imaging of bacteria; Tomography; FIB-SEM;
D O I
10.1016/j.jsb.2013.11.008
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
Efficient correlative imaging of small targets within large fields is a central problem in cell biology. Here, we demonstrate a series of technical advances in focused ion beam scanning electron microscopy (FIB-SEM) to address this issue. We report increases in the speed, robustness and automation of the process, and achieve consistent z slice thickness of similar to 3 nm. We introduce "keyframe imaging" as a new approach to simultaneously image large fields of view and obtain high-resolution 3D images of targeted sub-volumes. We demonstrate application of these advances to image post-fusion cytoplasmic intermediates of the HIV core. Using fluorescently labeled cell membranes, proteins and HIV cores, we first produce a "target map" of an HIV infected cell by fluorescence microscopy. We then generate a correlated 3D EM volume of the entire cell as well as high-resolution 3D images of individual HIV cores, achieving correlative imaging across a volume scale of 10(9) in a single automated experimental run. (C) 2014 Published by Elsevier Inc.
引用
收藏
页码:278 / 284
页数:7
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