Bullivant S, Ames A
J Cell Biol. 1966 Jun;29(3):435-47. doi: 10.1083/jcb.29.3.435.
A simple method to achieve results similar to the freeze-etching technique of Moor et al. (1961) is described. The frozen tissue is cut under liquid nitrogen with a razor blade outside the evaporator rather than inside with a cooled microtome. The conditions of the experiment do not favor sublimation, and it is proposed that the structure of the replica be explained by local faults in the cleavage plane which leaves structures, such as membranes, standing above the ice. Micrographs of replicas of glycerol-protected frozen small intestine of mouse prepared by the method are presented and the structural details they show are discussed. The problem of vapor-deposited contamination is discussed. It is concluded that this is a practical method for obtaining electron micrographs that are relatively free of artifact, and that further improvements may be expected from the use of rapidly frozen fresh tissue and a clean vacuum system, possibly of the ion-pumped type.
本文描述了一种能获得与莫尔等人(1961年)的冷冻蚀刻技术相似结果的简单方法。将冷冻组织在液氮下用剃须刀片在蒸发器外部而非在内部用冷却切片机切割。实验条件不利于升华,并且有人提出,复制品的结构可通过劈裂平面中的局部断层来解释,该断层会使诸如膜等结构留在冰之上。展示了用该方法制备的甘油保护的小鼠冷冻小肠复制品的显微照片,并讨论了它们所显示的结构细节。讨论了气相沉积污染问题。得出的结论是,这是一种获得相对无伪像的电子显微照片的实用方法,并且通过使用快速冷冻的新鲜组织和可能是离子泵型的清洁真空系统有望实现进一步改进。