Li Xinhui, Ji Tong, Hu Jun, Sun Jielin
Nanobiology Laboratory, Bio-X Life Science Research Center, School of Life Science and Biotechnology, Shanghai Jiao Tong University, 800 Dongchuan Road, Minhang District, Shanghai 200240, China.
Ultramicroscopy. 2008 Aug;108(9):826-31. doi: 10.1016/j.ultramic.2008.01.006. Epub 2008 Feb 14.
High resolution imaging of intracellular structures of ultrathin cell section samples is critical to the performance of precise manipulation by atomic force microscopy (AFM). Here, we test the effect of multiple factors during section sample preparation on the quality of the AFM image. These factors include the embedding materials, the annealing process of the specimen block, section thickness, and section side. We found that neither the embedding materials nor the temperature and speed of the annealing process has any effect on AFM image resolution. However, the section thickness and section side significantly affect the surface topography and AFM image resolution. By systematically testing the image quality of both sides of cell sections over a wide range of thickness (40-1000 nm), we found that the best resolution was obtained with upper-side sections approximately 50-100 nm thick. With these samples, we could observe precise structure details of the cell, including its membrane, nucleoli, and other organelles. Similar results were obtained for other cell types, including Tca8113, C6, and ECV-304. In brief, by optimizing the condition of ultrathin cell section preparation, we were able to obtain high resolution intracellular AFM images, which provide an essential basis for further AFM manipulation.
对超薄细胞切片样本的细胞内结构进行高分辨率成像对于原子力显微镜(AFM)进行精确操作至关重要。在此,我们测试了切片样本制备过程中多个因素对AFM图像质量的影响。这些因素包括包埋材料、样本块的退火过程、切片厚度和切片面。我们发现,包埋材料以及退火过程的温度和速度对AFM图像分辨率均无影响。然而,切片厚度和切片面会显著影响表面形貌和AFM图像分辨率。通过在较宽的厚度范围(40 - 1000 nm)内系统地测试细胞切片两面的图像质量,我们发现约50 - 100 nm厚的上表面切片能获得最佳分辨率。利用这些样本,我们能够观察到细胞的精确结构细节,包括其细胞膜、核仁及其他细胞器。对于其他细胞类型,包括Tca8113、C6和ECV - 304,也获得了类似结果。简而言之,通过优化超薄细胞切片制备条件,我们能够获得高分辨率的细胞内AFM图像,这为进一步的AFM操作提供了重要基础。