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生物标本的三维扫描透射电子显微镜观察。

Three-dimensional scanning transmission electron microscopy of biological specimens.

机构信息

Vanderbilt University Medical Center, Department of Molecular Physiology and Biophysics, Light Hall 702, Nashville, TN 37232-0615, USA.

出版信息

Microsc Microanal. 2010 Feb;16(1):54-63. doi: 10.1017/S1431927609991280.

Abstract

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.

摘要

已经从在经过像差校正扫描透射电子显微镜(STEM)中记录的焦平面系列图像中实现了哺乳动物细胞中的细胞骨架和网格蛋白包被陷窝的三维(3D)重建。该标本是生物结构的金属复制品,包括直径为 2-3nm 的 Pt 纳米颗粒,在电子束辐射下具有很高的稳定性。3D 数据集通过自动反卷积程序进行处理。横向分辨率为 1.1nm,由像素大小确定。仅在垂直位置相差 10nm 的颗粒被识别为彼此之间对比度下降超过 20%的单独物体。我们将此值称为反卷积或重建的轴向分辨率,即识别原始数据集中未解析的两个物体的能力。重建的分辨率可与通过倾斜系列透射电子显微镜获得的分辨率相媲美。然而,焦平面系列方法不需要机械倾斜,因此速度更快。还在包含 3T3 细胞的常规薄切片中记录了 Golgi 带的 3D STEM 图像,在反卷积数据集中具有可比的轴向分辨率。

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