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ultraLM and miniLM: Locator tools for smart tracking of fluorescent cells in correlative light and electron microscopy

机译:ultraLM和miniLM:用于在相关光学和电子显微镜中智能跟踪荧光细胞的定位器工具

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摘要

In-resin fluorescence (IRF) protocols preserve fluorescent proteins in resin-embedded cells and tissues for correlative light and electron microscopy, aiding interpretation of macromolecular function within the complex cellular landscape. Dual-contrast IRF samples can be imaged in separate fluorescence and electron microscopes, or in dual-modality integrated microscopes for high resolution correlation of fluorophore to organelle. IRF samples also offer a unique opportunity to automate correlative imaging workflows. Here we present two new locator tools for finding and following fluorescent cells in IRF blocks, enabling future automation of correlative imaging. The ultraLM is a fluorescence microscope that integrates with an ultramicrotome, which enables ‘smart collection’ of ultrathin sections containing fluorescent cells or tissues for subsequent transmission electron microscopy or array tomography. The miniLM is a fluorescence microscope that integrates with serial block face scanning electron microscopes, which enables ‘smart tracking’ of fluorescent structures during automated serial electron image acquisition from large cell and tissue volumes.
机译:树脂内荧光(IRF)协议将荧光蛋白保留在树脂包埋的细胞和组织中,以进行相关的光镜和电子显微镜检查,有助于解释复杂细胞环境中的大分子功能。可以在单独的荧光显微镜和电子显微镜中或在双模态集成显微镜中对双对比IRF样品成像,以实现荧光团与细胞器的高分辨率关联。 IRF样本还为自动化相关成像工作流程提供了独特的机会。在这里,我们介绍了两个新的定位器工具,用于查找和跟踪IRF块中的荧光细胞,从而使相关成像的未来自动化成为可能。 ultraLM是与超薄切片机集成在一起的荧光显微镜,可以“智能收集”包含荧光细胞或组织的超薄切片,以便随后进行透射电子显微镜或阵列层析成像。 miniLM是与串行块面扫描电子显微镜集成的荧光显微镜,可在从大量细胞和组织中自动采集串行电子图像期间对荧光结构进行“智能跟踪”。

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