Correlative Fluorescence and Electron Microscopy in 3D—Scanning Electron Microscope Perspective

Q1 Health Professions
Jonathan Franks, Callen T. Wallace, Masateru Shibata, Mitsuo Suga, Natasha Erdman, Donna B. Stolz, Simon C. Watkins
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引用次数: 4

Abstract

The ability to correlate fluorescence microscopy (FM) and electron microscopy (EM) data obtained on biological (cell and tissue) specimens is essential to bridge the resolution gap between the data obtained by these different imaging techniques. In the past such correlations were limited to either EM navigation in two dimensions to the locations previously highlighted by fluorescence markers, or subsequent high-resolution acquisition of tomographic information using a TEM. We present a novel approach whereby a sample previously investigated by FM is embedded and subjected to sequential mechanical polishing and backscatter imaging by scanning electron microscope. The resulting three dimensional EM tomogram of the sample can be directly correlated to the FM data. © 2017 by John Wiley & Sons, Inc.

三维扫描电镜视角下的相关荧光与电子显微镜
将生物(细胞和组织)标本上获得的荧光显微镜(FM)和电子显微镜(EM)数据关联起来的能力对于弥合这些不同成像技术获得的数据之间的分辨率差距至关重要。在过去,这种相关性被限制在二维EM导航到荧光标记先前突出显示的位置,或随后使用TEM获得高分辨率层析成像信息。我们提出了一种新的方法,即将先前由FM研究的样品嵌入并通过扫描电子显微镜进行顺序机械抛光和背散射成像。所得样品的三维EM层析图可以直接与FM数据相关。©2017 by John Wiley &儿子,Inc。
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来源期刊
Current Protocols in Cytometry
Current Protocols in Cytometry Health Professions-Medical Laboratory Technology
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期刊介绍: Published in affiliation with the International Society for Advancement of Cytometry, Current Protocols in Cytometry is a "best practices" collection that distills and organizes the absolute latest techniques from the top cytometry labs and specialists worldwide. It is the most complete set of peer-reviewed protocols for flow and image cytometry available.
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