Department of Biology and Howard Hughes Medical Institute, University of Utah, Salt Lake City, Utah, USA.
Nat Methods. 2011 Jan;8(1):80-4. doi: 10.1038/nmeth.1537. Epub 2010 Nov 21.
A complete portrait of a cell requires a detailed description of its molecular topography: proteins must be linked to particular organelles. Immunocytochemical electron microscopy can reveal locations of proteins with nanometer resolution but is limited by the quality of fixation, the paucity of antibodies and the inaccessibility of antigens. Here we describe correlative fluorescence electron microscopy for the nanoscopic localization of proteins in electron micrographs. We tagged proteins with the fluorescent proteins Citrine or tdEos and expressed them in Caenorhabditis elegans, fixed the worms and embedded them in plastic. We imaged the tagged proteins from ultrathin sections using stimulated emission depletion (STED) microscopy or photoactivated localization microscopy (PALM). Fluorescence correlated with organelles imaged in electron micrographs from the same sections. We used these methods to localize histones, a mitochondrial protein and a presynaptic dense projection protein in electron micrographs.
要全面描绘一个细胞,需要详细描述其分子拓扑结构:蛋白质必须与特定的细胞器相连。免疫细胞化学电子显微镜可以揭示蛋白质的位置,分辨率达到纳米级,但受到固定质量、抗体缺乏和抗原不可及性的限制。在这里,我们描述了用于在电子显微镜照片中纳米尺度定位蛋白质的相关荧光电子显微镜。我们使用荧光蛋白 Citrine 或 tdEos 标记蛋白质,并在秀丽隐杆线虫中表达它们,固定蠕虫并将其嵌入塑料中。我们使用受激发射损耗 (STED) 显微镜或光激活定位显微镜 (PALM) 从超薄切片中对标记的蛋白质进行成像。荧光与来自同一切片的电子显微镜图像中成像的细胞器相吻合。我们使用这些方法在电子显微镜图像中定位组蛋白、线粒体蛋白和突触前致密投射蛋白。