Central Facility for Electron Microscopy, Ulm University, 89069 Ulm, Germany.
Histochem Cell Biol. 2012 Oct;138(4):549-56. doi: 10.1007/s00418-012-1020-6. Epub 2012 Aug 25.
Focused ion beam/scanning electron microscopy (FIB/SEM) tomography is a novel powerful approach for three-dimensional (3D) imaging of biological samples. Thereby, a sample is repeatedly milled with the focused ion beam (FIB) and each newly produced block face is imaged with the scanning electron microscope (SEM). This process can be repeated ad libitum in arbitrarily small increments allowing 3D analysis of relatively large volumes such as eukaryotic cells. High-pressure freezing and freeze substitution, on the other hand, are the gold standards for electron microscopic preparation of whole cells. In this work, we combined these methods and substantially improved resolution by using the secondary electron signal for image formation. With this imaging mode, contrast is formed in a very small, well-defined area close to the newly produced surface. By using this approach, small features, so far only visible in transmission electron microscope (TEM) (e.g., the two leaflets of the membrane bi-layer, clathrin coats and cytoskeletal elements), can be resolved directly in the FIB/SEM in the 3D context of whole cells.
聚焦离子束/扫描电子显微镜(FIB/SEM)断层扫描是一种用于生物样本三维(3D)成像的新型强大方法。在此过程中,样品会被聚焦离子束(FIB)反复铣削,并且每个新生成的块状面都会用扫描电子显微镜(SEM)成像。该过程可以任意地以非常小的增量重复进行,从而可以对相对较大的体积(如真核细胞)进行 3D 分析。另一方面,高压冷冻和冷冻替代是整个细胞电子显微镜制备的金标准。在这项工作中,我们结合了这些方法,并通过使用二次电子信号进行图像形成,大大提高了分辨率。在这种成像模式下,对比度是在非常小的、定义明确的靠近新生成表面的区域中形成的。通过使用这种方法,可以直接在 FIB/SEM 中在整个细胞的 3D 环境中解析出迄今为止只能在透射电子显微镜(TEM)中看到的小特征(例如,膜双层的两个小叶、网格蛋白外壳和细胞骨架元素)。