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Correlative microscopy methods that maximize specimen fidelity and data completeness, and improve molecular localization capabilities

机译:相关显微镜方法可最大程度地提高样品保真度和数据完整性,并提高分子定位能力

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摘要

Correlative microscopy techniques interrogate biological systems more thoroughly than is possible using a single modality. This is particularly true if disparate data types can be acquired from the same specimen. Recently, there has been significant progress towards combining the structural information obtained from soft X-ray tomography (SXT) with molecular localization data. Here we will compare methods for determining the position of molecules in a cell viewed by SXT, including direct visualization using electron dense labels, and by indirect methods, such as fluorescence microscopy and high numerical aperture cryo-light microscopy. We will also discuss available options for preserving the in vivo structure and organization of the specimen during multi-modal data collection, and how some simple specimen mounting concepts can ensure maximal data completeness in correlative imaging experiments. (c) 2013 Elsevier Inc. All rights reserved.
机译:相关的显微镜技术比使用单一模式可能更彻底地检查生物系统。如果可以从同一样本中获取不同的数据类型,则尤其如此。最近,在将从软X射线断层扫描(SXT)获得的结构信息与分子定位数据相结合方面取得了重大进展。在这里,我们将比较确定分子在SXT中观察到的分子位置的方法,包括使用电子致密标记物的直接可视化,以及通过间接方法(例如荧光显微镜和高数值孔径冷冻光显微镜)进行的可视化。我们还将讨论在多模式数据收集过程中保留标本的体内结构和组织的可用选项,以及一些简单的标本安装概念如何在相关成像实验中确保最大程度的数据完整性。 (c)2013 Elsevier Inc.保留所有权利。

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