Computer image processing of electron micrographs of biological structures with helical symmetry.

M Stewart
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引用次数: 70

Abstract

Methods are described for the analysis of electron micrographs of biological objects with helical symmetry and for the production of three-dimensional models of these structures using computer image reconstruction methods. Fourier-based processing of one- and two-dimensionally ordered planar arrays is described by way of introduction, before analysing the special properties of helices and their transforms. Conceiving helical objects as a sum of helical waves (analogous to the sum of planar waves used to describe a planar crystal) is shown to facilitate analysis and enable three-dimensional models to be produced, often from a single view of the object. The corresponding Fourier transform of such a sum of helical waves consists of a sum of Bessel function terms along layer lines. Special problems deriving from the overlapping along layer lines of terms of different Bessel order are discussed, and methods to separate these terms, based on analysing a number of different azimuthal views of the object by least squares, are described. Corrections to alleviate many technical and specimen-related problems are discussed in conjunction with a consideration of the computer methods used to actually process an image. A range of examples of helical objects, including viruses, microtubules, flagella, actin, and myosin filaments, are discussed to illustrate the range of problems that can be addressed by computer reconstruction methods.

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螺旋对称生物结构电子显微图的计算机图像处理。
方法描述了对具有螺旋对称的生物物体的电子显微图的分析,以及使用计算机图像重建方法产生这些结构的三维模型。在分析螺旋及其变换的特殊性质之前,以介绍的方式描述了一维和二维有序平面阵列的傅里叶处理。将螺旋物体设想为螺旋波的总和(类似于用于描述平面晶体的平面波的总和)被证明有助于分析并使三维模型能够产生,通常是从物体的单一视图。相应的螺旋波和的傅里叶变换由沿层线的贝塞尔函数项和组成。讨论了不同贝塞尔阶项沿层线重叠所引起的特殊问题,并描述了利用最小二乘法分析物体若干不同方位角视图的分离这些项的方法。修正,以减轻许多技术和标本相关的问题,讨论结合考虑计算机方法用于实际处理图像。讨论了一系列螺旋状物体的例子,包括病毒、微管、鞭毛、肌动蛋白和肌凝蛋白丝,以说明可以通过计算机重建方法解决的问题范围。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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Real time computer simulation of transmission electron microscope images with tilted illumination: grain boundary applications. Cryofixation of vascular endothelium. The endothelial vesicle system in cryofixed frog mesenteric capillaries analysed by ultrathin serial sectioning. Lectin and immunolabeling of microvascular endothelia. Quick-freeze, deep-etch studies of endothelial components, with special reference to cytoskeletons and vesicle structures.
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