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Quantitating morphological changes in biological samples during scanning electron microscopy sample preparation with correlative super-resolution microscopy

机译:使用相关超分辨率显微镜定量扫描电子显微镜样品制备过程中生物样品的形态变化

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摘要

Sample preparation is critical to biological electron microscopy (EM), and there have been continuous efforts on optimizing the procedures to best preserve structures of interest in the sample. However, a quantitative characterization of the morphological changes associated with each step in EM sample preparation is currently lacking. Using correlative EM and superresolution microscopy (SRM), we have examined the effects of different drying methods as well as osmium tetroxide (OsO4) post-fixation on cell morphology during scanning electron microscopy (SEM) sample preparation. Here, SRM images of the sample acquired under hydrated conditions were used as a baseline for evaluating morphological changes as the sample went through SEM sample processing. We found that both chemical drying and critical point drying lead to a mild cellular boundary retraction of ~60 nm. Post-fixation by OsO4 causes at least 40 nm additional boundary retraction. We also found that coating coverslips with adhesion molecules such as fibronectin prior to cell plating helps reduce cell distortion from OsO4 post-fixation. These quantitative measurements offer useful information for identifying causes of cell distortions in SEM sample preparation and improving current procedures.
机译:样品制备对生物电子显微镜(EM)至关重要,并且一直在努力优化程序以最好地保存样品中感兴趣的结构。但是,目前尚缺乏与EM样品制备中每个步骤相关的形态变化的定量表征。使用相关的EM和超分辨率显微镜(SRM),我们在扫描电子显微镜(SEM)样品制备过程中研究了不同的干燥方法以及四氧化(OsO4)后固定对细胞形态的影响。在此,将在水合条件下采集的样品的SRM图像用作评估样品经过SEM样品处理时的形态变化的基准。我们发现化学干燥和临界点干燥都会导致〜60 nm的温和细胞边界收缩。 OsO4的后固定会导致至少40 nm的额外边界收缩。我们还发现,在细胞铺板前用黏附分子(例如纤连蛋白)涂覆盖玻片有助于减少OsO4固定后的细胞变形。这些定量测量提供了有用的信息,可用于确定SEM样品制备中细胞变形的原因并改进当前的程序。

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