Fukuda Yoshiyuki, Schrod Nikolas, Schaffer Miroslava, Feng Li Rebekah, Baumeister Wolfgang, Lucic Vladan
Max-Planck-Institute of Biochemistry, Am Klopferspitz 18, 82152 Martinsried, Germany.
Max-Planck-Institute of Biochemistry, Am Klopferspitz 18, 82152 Martinsried, Germany.
Ultramicroscopy. 2014 Aug;143:15-23. doi: 10.1016/j.ultramic.2013.11.008. Epub 2013 Dec 1.
Correlative microscopy allows imaging of the same feature over multiple length scales, combining light microscopy with high resolution information provided by electron microscopy. We demonstrate two procedures for coordinate transformation based correlative microscopy of vitrified biological samples applicable to different imaging modes. The first procedure aims at navigating cryo-electron tomography to cellular regions identified by fluorescent labels. The second procedure, allowing navigation of focused ion beam milling to fluorescently labeled molecules, is based on the introduction of an intermediate scanning electron microscopy imaging step to overcome the large difference between cryo-light microscopy and focused ion beam imaging modes. These methods make it possible to image fluorescently labeled macromolecular complexes in their natural environments by cryo-electron tomography, while minimizing exposure to the electron beam during the search for features of interest.
相关显微镜技术能够在多个长度尺度上对同一特征进行成像,它将光学显微镜与电子显微镜提供的高分辨率信息相结合。我们展示了两种基于坐标变换的相关显微镜技术程序,适用于不同成像模式的玻璃化生物样品。第一种程序旨在将冷冻电子断层扫描引导至由荧光标记识别的细胞区域。第二种程序基于引入中间扫描电子显微镜成像步骤,以克服冷冻光学显微镜和聚焦离子束成像模式之间的巨大差异,从而实现将聚焦离子束铣削引导至荧光标记分子。这些方法使得通过冷冻电子断层扫描在其自然环境中对荧光标记的大分子复合物进行成像成为可能,同时在寻找感兴趣特征的过程中尽量减少电子束的暴露。