Bellare J R, Davis H T, Scriven L E, Talmon Y
Department of Chemical Engineering & Materials Science, University of Minnesota, Minneapolis 55455-0132.
J Electron Microsc Tech. 1988 Sep;10(1):87-111. doi: 10.1002/jemt.1060100111.
The controlled environment vitrification system (CEVS) permits cryofixation of hydrated biological and colloidal dispersions and aggregates from a temperature- and saturation-controlled environment. Otherwise, specimens prepared in an uncontrolled laboratory atmosphere are subject to evaporation and heat transfer, which may introduce artifacts caused by concentration, pH, ionic strength, and temperature changes. Moreover, it is difficult to fix and examine the microstructure of systems at temperatures other than ambient (e.g., biological systems at in vivo conditions and colloidal systems above room temperature). A system has been developed that ensures that a liquid or partially liquid specimen is maintained in its original state while it is being prepared before vitrification and, once prepared, is vitrified with little alteration of its microstructure. A controlled environment is provided within a chamber where temperature and chemical activity of volatile components can be controlled while the specimen is being prepared. The specimen grid is mounted on a plunger, and a synchronous shutter is opened almost simultaneously with the release of the plunger, so that the specimen is propelled abruptly through the shutter opening into a cryogenic bath. We describe the system and its use and illustrate the value of the technique with TEM micrographs of surfactant microstructures in which specimen preparation artifacts were avoided. We also discuss applications to other instruments like SEM, to other techniques like freeze-fracture, and to novel "on the grid" experiments that make it possible to freeze successive instants of dynamic processes such as membrane fusion, chemical reactions, and phase transitions.
可控环境玻璃化系统(CEVS)能够在温度和饱和度可控的环境下对含水的生物及胶体分散体与聚集体进行冷冻固定。否则,在不受控的实验室环境中制备的标本会受到蒸发和热传递的影响,这可能会引入因浓度、pH值、离子强度和温度变化而导致的假象。此外,在环境温度以外的其他温度下(例如,处于体内条件的生物系统和高于室温的胶体系统),很难固定和检查系统的微观结构。现已开发出一种系统,该系统可确保液体或部分液体标本在玻璃化前的制备过程中保持其原始状态,并且一旦制备完成,其微观结构几乎不会改变地被玻璃化。在标本制备过程中,在一个腔室内提供可控环境,在该腔室内可控制挥发性成分的温度和化学活性。标本网格安装在一个柱塞上,并且一个同步快门几乎与柱塞的释放同时打开,以便标本通过快门开口突然被推进到低温浴中。我们描述了该系统及其用途,并用避免了标本制备假象的表面活性剂微观结构的透射电子显微镜照片说明了该技术的价值。我们还讨论了该系统在扫描电子显微镜等其他仪器、冷冻断裂等其他技术以及新型“网格上”实验中的应用,这些实验使得冻结诸如膜融合、化学反应和相变等动态过程的连续瞬间成为可能。