Three-Dimensional Scanning Transmission Electron Microscopy of Biological Specimens

被引:35
作者
de Jonge, Niels [1 ,2 ]
Sougrat, Rachid [3 ]
Northan, Brian M. [4 ]
Pennycook, Stephen J. [2 ]
机构
[1] Vanderbilt Univ, Dept Mol Physiol & Biophys, Med Ctr, Nashville, TN 37232 USA
[2] Oak Ridge Natl Lab, Div Mat Sci & Technol, Oak Ridge, TN 37831 USA
[3] NICHD, Cell Biol & Metab Branch, NIH, Bethesda, MD 20892 USA
[4] Media Cybernet Inc, Bethesda, MD 20814 USA
基金
美国国家卫生研究院;
关键词
three-dimensional electron microscopy; aberration-corrected STEM; biological electron microscopy; thin sections; cytoskeleton; clathrin-coated pit; deconvolution; nanoparticles; VISUALIZATION; CELLS;
D O I
10.1017/S1431927609991280
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A three-dimensional (3D) reconstruction of the cytoskeleton and a clathrin-coated pit in mammalian cells has been achieved from a focal-series of images recorded in an aberration-corrected scanning transmission electron microscope (STEM). The specimen was a metallic replica of the biological structure comprising Pt nanoparticles 2-3 nm in diameter, with a high stability under electron beam radiation. The 3D dataset was processed by an automated deconvolution procedure. The lateral resolution was 1.1 nm, set by pixel size. Particles differing by only 10 nm in vertical position were identified as separate objects with greater than 20% dip in contrast between them. We refer to this value as the axial resolution of the deconvolution or reconstruction, the ability to recognize two objects, which were unresolved in the original dataset. The resolution of the reconstruction is comparable to that achieved by tilt-series transmission electron microscopy. However, the focal-series method does not require mechanical tilting and is therefore much faster. 3D STEM images were also recorded of the Golgi ribbon in conventional thin sections containing 3T3 cells with a comparable axial resolution in the deconvolved dataset.
引用
收藏
页码:54 / 63
页数:10
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