Liquid Scanning Transmission Electron Microscopy: Imaging Protein Complexes in their Native Environment in Whole Eukaryotic Cells

被引:43
作者
Peckys, Diana B. [1 ]
de Jonge, Niels [1 ,2 ]
机构
[1] Leibniz Inst New Mat INM, D-66123 Saarbrucken, Germany
[2] Vanderbilt Univ, Dept Mol Physiol & Biophys, Sch Med, Nashville, TN 37232 USA
关键词
Liquid STEM; ESEM-STEM; gold nanoparticle; specific label; epidermal growth factor receptor (EGFR); whole cell; live cell microscopy; environmental scanning electron microscopy; GOLD NANOPARTICLE UPTAKE; PLASMA-MEMBRANE; SIGNAL-TRANSDUCTION; CELLULAR UPTAKE; WET-CELL; GROWTH; RESOLUTION; EGF; SPECIMENS; STEM;
D O I
10.1017/S1431927614000099
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Scanning transmission electron microscopy (STEM) of specimens in liquid, so-called Liquid STEM, is capable of imaging the individual subunits of macromolecular complexes in whole eukaryotic cells in liquid. This paper discusses this new microscopy modality within the context of state-of-the-art microscopy of cells. The principle of operation and equations for the resolution are described. The obtained images are different from those acquired with standard transmission electron microscopy showing the cellular ultrastructure. Instead, contrast is obtained on specific labels. Images can be recorded in two ways, either via STEM at 200 keV electron beam energy using a microfluidic chamber enclosing the cells, or via environmental scanning electron microscopy at 30 keV of cells in a wet environment. The first series of experiments involved the epidermal growth factor receptor labeled with gold nanoparticles. The labels were imaged in whole fixed cells with nanometer resolution. Since the cells can be kept alive in the microfluidic chamber, it is also feasible to detect the labels in unfixed, live cells. The rapid sample preparation and imaging allows studies of multiple whole cells.
引用
收藏
页码:346 / 365
页数:20
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