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- W2026005691 abstract "Visualization of cellular processes at a resolution of the individual protein should involve integrative and complementary approaches that can eventually draw realistic functional and cellular landscapes. Electron tomography of vitrified but otherwise unaltered cells emerges as a central method for three-dimensional reconstruction of cellular architecture at a resolution of 2–6 nm. While a combination of correlative light-based microscopy with cryo-electron tomography (cryo-ET) provides medium-resolution insight into pivotal cellular processes, fitting high-resolution structural approaches, for example, X-ray crystallography, into reconstructed macromolecular assemblies provides unprecedented information on native protein assemblies. Thus, cryo-ET bridges the resolution gap between cellular and structural biology. In this article, we focus on the study of eukaryotic cells and macromolecular complexes in a close-to-life-state. We discuss recent developments and structural findings enabling major strides to be made in understanding complex physiological functions." @default.
- W2026005691 created "2016-06-24" @default.
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- W2026005691 date "2011-10-01" @default.
- W2026005691 modified "2023-10-17" @default.
- W2026005691 title "Cryo-electron tomography: gaining insight into cellular processes by structural approaches" @default.
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- W2026005691 doi "https://doi.org/10.1016/j.sbi.2011.07.004" @default.
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