Three-dimensional electron microscopy at molecular resolution.

Sriram Subramaniam, Jacqueline L S Milne
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引用次数: 76

Abstract

Emerging methods in cryo-electron microscopy allow determination of the three-dimensional architectures of objects ranging in size from small proteins to large eukaryotic cells, spanning a size range of more than 12 orders of magnitude. Advances in determining structures by "single particle" microscopy and by "electron tomography" provide exciting opportunities to describe the structures of subcellular assemblies that are either too large or too heterogeneous to be investigated by conventional crystallographic methods. Here, we review selected aspects of progress in structure determination by cryo-electron microscopy at molecular resolution, with a particular emphasis on topics at the interface of single particle and tomographic approaches. The rapid pace of development in this field suggests that comprehensive descriptions of the structures of whole cells and organelles in terms of the spatial arrangements of their molecular components may soon become routine.

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分子分辨率的三维电子显微镜。
低温电子显微镜中的新兴方法允许确定从小蛋白质到大真核细胞的物体的三维结构,跨越超过12个数量级的尺寸范围。通过“单粒子”显微镜和“电子断层扫描”确定结构的进展为描述亚细胞组件的结构提供了令人兴奋的机会,这些结构要么太大,要么太不均匀,无法用传统的晶体学方法进行研究。在这里,我们回顾了低温电子显微镜在分子分辨率下结构测定方面的进展,特别强调了单粒子和层析方法界面的主题。这一领域的快速发展表明,根据分子组分的空间排列来全面描述整个细胞和细胞器的结构可能很快就会成为常规。
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Visualizing flexibility at molecular resolution: analysis of heterogeneity in single-particle electron microscopy reconstructions. Phase boundaries and biological membranes. Calculation of protein-ligand binding affinities. Synthetic gene circuits: design with directed evolution. Bilayer thickness and membrane protein function: an energetic perspective.
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