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高压冷冻、细胞断层扫描与结构细胞生物学

High-pressure freezing, cellular tomography, and structural cell biology.

作者信息

McDonald Kent L, Auer Manfred

机构信息

Electron Microscope Laboratory, University of California, Berkeley, USA.

出版信息

Biotechniques. 2006 Aug;41(2):137, 139, 141 passim. doi: 10.2144/000112226.

Abstract

Structural cell biology, which we define as electron microscopic analysis of intact cells, suffered a loss of interest and activity following the advances in light microscopy beginning in the 1990s. Interestingly, it is the wealth of detailed observation in the light microscope that is one of the driving forces for the current renewed interest in electron microscopy (EM). A great many cellular details are simply beyond the resolving power of the light microscope. In this article, we describe how electron microscopists are responding to the demands for better preservation of cells and for ways to view cell ultrastructure in three dimensions at high resolution. We discuss how low temperature methods, especially high-pressure freezing and freeze substitution, reduce the artifacts of conventional EM specimen preparation. We also give a brief introduction to cellular electron tomography, a powerful analytical method that can give near-atomic resolution of cell ultrastructure in three-dimensional (3-D) models.

摘要

结构细胞生物学,我们将其定义为对完整细胞的电子显微镜分析,在20世纪90年代开始的光学显微镜技术进步之后,受到了关注和研究活动的减少。有趣的是,正是光学显微镜中丰富的详细观察结果,成为了当前对电子显微镜(EM)重新产生兴趣的驱动力之一。许多细胞细节完全超出了光学显微镜的分辨率。在本文中,我们描述了电子显微镜学家如何应对更好地保存细胞以及在高分辨率下以三维方式观察细胞超微结构的需求。我们讨论了低温方法,特别是高压冷冻和冷冻置换,如何减少传统电子显微镜标本制备中的假象。我们还简要介绍了细胞电子断层扫描,这是一种强大的分析方法,可以在三维(3-D)模型中给出接近原子分辨率的细胞超微结构。

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