Tsuji Takuma, Fujimoto Toyoshi
Department of Anatomy and Molecular Cell Biology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Bio Protoc. 2017 Sep 20;7(18):e2556. doi: 10.21769/BioProtoc.2556.
We describe a streamlined method that enables the quick observation of yeast ultrastructure by electron microscopy (EM). Yeast cells are high-pressure frozen, freeze-fractured to cut across the cytoplasm, and freeze-etched to sublimate ice in the cytosol and the organelle lumen. The cellular structures delineated by these procedures are coated by a thin layer of platinum and carbon deposited by vacuum evaporation, and this platinum-carbon layer, or replica, is observed by transmission EM. The method differs from the deep-etching of pre-extracted samples in that intact live cells are processed without any chemical treatment. Lipid droplets made of unetchable lipid esters are observed most prominently, but other organelles-the nucleus, endoplasmic reticulum, Golgi, vacuoles, mitochondria-and their mutual relationships can be analyzed readily. It is of note that the entire procedure, from quick-freezing to EM observation, can be performed within a day.
我们描述了一种简化方法,可通过电子显微镜(EM)快速观察酵母超微结构。酵母细胞先进行高压冷冻,然后进行冷冻断裂以横穿细胞质,再进行冷冻蚀刻以使细胞质溶胶和细胞器内腔中的冰升华。通过这些步骤勾勒出的细胞结构被通过真空蒸发沉积的一层薄铂和碳覆盖,然后通过透射电子显微镜观察这层铂 - 碳层,即复制品。该方法与预提取样品的深度蚀刻不同,因为完整的活细胞无需任何化学处理即可进行处理。由不可蚀刻的脂质酯构成的脂滴最为显著地被观察到,但其他细胞器——细胞核、内质网、高尔基体、液泡、线粒体——及其相互关系也能很容易地进行分析。值得注意的是,从快速冷冻到电子显微镜观察的整个过程可以在一天内完成。