Image analysis of single macromolecules

Joachim Frank
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引用次数: 45

Abstract

A battery of sophisticated techniques is now available to extract three-dimensional structural information from electron micrographs of biological macromolecules occurring in the form of single particles. One of these techniques, the random-conical reconstruction method, which allows low-dose imaging, has been recently perfected and is being used routinely for the study of ribosomal architecture. The analysis of the 40S mammalian ribosomal subunit serves as an illustration of the various steps of image processing. The use of classification combined with 3-D reconstruction provides the means to investigate variations of the macromolecular structure (deformations, conformational changes, etc.) that are caused by the specimen preparation. An example is provided by the changes in the shape of the 70S monosome of E. coli as it changes its orientation on the carbon grid. The most challenging applications of the techniques discussed are in the area of cryo-microscopy of ice-embedded specimens. First studies of single macromolecules imaged in this way have indicated that the 3-D imaging methods and, specifically, the random-conical reconstruction method, will be applicable under these conditions.

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单个大分子的图像分析
现在有一系列复杂的技术可以从以单个粒子形式出现的生物大分子的电子显微照片中提取三维结构信息。其中一种技术,随机锥形重建法,允许低剂量成像,最近已经完善,并被常规用于核糖体结构的研究。对40S哺乳动物核糖体亚基的分析说明了图像处理的各个步骤。使用分类与三维重建相结合的方法提供了研究由样品制备引起的大分子结构(变形,构象变化等)变化的手段。大肠杆菌的70S单体在改变其在碳网格上的方向时形状的变化提供了一个例子。所讨论的技术最具挑战性的应用是在冰包埋标本的冷冻显微镜领域。首次用这种方法对单个大分子成像的研究表明,三维成像方法,特别是随机锥形重建方法,将适用于这些条件。
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