Leis Andrew, Rockel Beate, Andrees Lars, Baumeister Wolfgang
Max Planck Institute of Biochemistry, Department of Molecular Structural Biology, Am Klopferspitz 18, D-82152 Martinsried, Germany.
Trends Biochem Sci. 2009 Feb;34(2):60-70. doi: 10.1016/j.tibs.2008.10.011. Epub 2008 Dec 26.
Cryogenic electron tomography (cryo- ET) enables the 3D visualization of biological material at a previously unseeable scale. Carefully controlled cryogenic specimen preparation avoids the artefacts that are notorious to conventional electron microscopy specimen preparation. To date, studies employing cryo- ET have mostly been restricted to isolated macromolecular assemblies, small prokaryotic cells or thin regions of eukaryotic cells owing to the limited penetration depth of electrons through ice-embedded preparations. Recent progress in cryosectioning makes it possible to acquire tomograms from many kinds of vitrified cells and tissues. The systematic and comprehensive interpretation of such tomograms will provide unprecedented insight into the molecular organization of cellular landscapes.
低温电子断层扫描(cryo-ET)能够以前所未有的尺度对生物材料进行三维可视化。精心控制的低温样本制备可避免传统电子显微镜样本制备中常见的伪像。迄今为止,由于电子穿过冷冻包埋样本的穿透深度有限,采用cryo-ET的研究大多局限于分离的大分子组装体、小型原核细胞或真核细胞的薄区域。冷冻切片技术的最新进展使得从多种玻璃化细胞和组织中获取断层扫描图像成为可能。对这些断层扫描图像进行系统而全面的解读将为细胞景观的分子组织提供前所未有的见解。