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Building the atomic model for the bacterial flagellar filament by electron cryomicroscopy and image analysis

机译:通过电子显微镜和图像分析建立细菌鞭毛丝的原子模型

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The bacterial flagellar filament is a helical propeller for bacterial locomotion. It is a well-ordered helical assembly of a single protein, flagellin, and its tubular structure is formed by 11 protofilaments, each in either of the two distinct conformations, L- and R-type, for supercoiling. We have been studying the three-dimensional structures of the flagellar filaments by electron cryomicroscopy and recently obtained a density map of the R-type filament up to 4 A resolution from an image data set containing only about 41,000 molecular images. The density map showed the features of the alpha-helical backbone and some large side chains, which allowed us to build the complete atomic model as one of the first atomic models of macromolecules obtained solely by electron microscopy image analysis (Yonekura et al., 2003a). We briefly review the structure and the structure analysis, and point out essential techniques that have made this analysis possible.
机译:细菌鞭毛细丝是用于细菌运动的螺旋桨。它是单个蛋白质鞭毛蛋白的有序螺旋状装配,其管状结构由11个原丝形成,每个原丝都具有两种不同的构型(L型和R型),用于超螺旋。我们已经通过电子冷冻显微镜研究了鞭毛丝的三维结构,最近从仅包含约41,000个分子图像的图像数据集中获得了分辨率高达4 A的R型丝的密度图。密度图显示了α-螺旋骨架和一些大侧链的特征,这使我们能够建立完整的原子模型,作为仅通过电子显微镜图像分析获得的大分子的首批原子模型之一(Yonekura等人,2003a )。我们简要回顾一下结构和结构分析,并指出使该分析成为可能的基本技术。

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