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冷冻超薄切片术:玻璃体切片的冷冻电子显微镜检查

Cryoultramicrotomy: cryoelectron microscopy of vitreous sections.

作者信息

Vanhecke Dimitri, Studer Luca, Studer Daniel

机构信息

Institut für Anatomie, University of Bern, Switzerland.

出版信息

Methods Mol Biol. 2007;369:175-97. doi: 10.1007/978-1-59745-294-6_9.

Abstract

Cryoultramicrotomy allows the sectioning of vitrified biological samples. These biological samples are preserved at the atomic level and represent the real structure at the moment of freezing. Cryoultramicrotomy produces ultra-thin cryosections that are investigated in a cryoelectron microscope. The necessity of working during the whole preparation at temperatures less than -140 degrees C results in some difficulties, including the cryosection transfer from the knife-edge to the electron microscropy grid; the grid handling in the cryochamber and the grid transfer into the cryoholder of the electron microscope. Furthermore, ice crystal contamination (from air humidity) can obscure the structures of interest in the sections. It is mainly know-how and experience that will prevent the contamination of ice crystals and the recrystallization of the sections during the manipulations. Here, we describe the tips, tricks, the tools, and methods that help to overcome these burdens and pave the path for successful cryoultramicrotomy.

摘要

低温超薄切片术可对玻璃化生物样品进行切片。这些生物样品在原子水平上得以保存,呈现出冷冻瞬间的真实结构。低温超薄切片术可制作超薄冷冻切片,用于在冷冻电子显微镜下进行研究。在整个制备过程中都需要在低于 -140摄氏度的温度下操作,这带来了一些困难,包括将冷冻切片从刀刃转移到电子显微镜载网;在冷冻室中处理载网以及将载网转移到电子显微镜的冷冻样品夹中。此外,(来自空气湿度的)冰晶污染可能会模糊切片中感兴趣的结构。主要依靠专业知识和经验来防止在操作过程中出现冰晶污染和切片重结晶。在此,我们描述一些技巧、窍门、工具和方法,以帮助克服这些困难,为成功进行低温超薄切片术铺平道路。

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