Lucić Vladan, Förster Friedrich, Baumeister Wolfgang
Department of Structural Biology, Max Planck Institute of Biochemistry, D-82152 Martinsried, Germany.
Annu Rev Biochem. 2005;74:833-65. doi: 10.1146/annurev.biochem.73.011303.074112.
Electron tomography (ET) is uniquely suited to obtain three-dimensional reconstructions of pleomorphic structures, such as cells, organelles or supramolecular assemblies. Although the principles of ET have been known for decades, its use has gathered momentum only in recent years, thanks to technological advances and its combination with improved specimen preparation techniques. The rapid freezing/freeze-substitution preparation is applicable to whole cells and tissues, and it is the method of choice for ET investigations of cellular ultrastructure. The frozen-hydrated preparation provides the best possible structural preservation and allows the imaging of molecules, complexes, and supramolecular assemblies in their native state and their natural environment. Devoid of staining and chemical fixation artifacts, cryo-ET provides a faithful representation of both the surface and internal structure of molecules. In combination with advanced computational methods, such as molecular identification based on pattern recognition techniques, cryo-ET is currently the most promising approach to comprehensively map macromolecular architecture inside cellular tomograms.
电子断层扫描(ET)特别适合用于获取多形结构的三维重建,如细胞、细胞器或超分子组装体。尽管ET的原理已为人所知数十年,但由于技术进步以及它与改进的样品制备技术相结合,其应用仅在近年来才得到迅速发展。快速冷冻/冷冻置换制备适用于整个细胞和组织,是ET研究细胞超微结构的首选方法。冷冻水合制备能提供尽可能好的结构保存,并允许在分子、复合物和超分子组装体的天然状态及其自然环境中对其进行成像。冷冻电镜断层扫描(cryo-ET)没有染色和化学固定伪像,能忠实地呈现分子的表面和内部结构。结合先进的计算方法,如基于模式识别技术的分子识别,cryo-ET目前是全面绘制细胞断层图像中大分子结构的最有前景的方法。