Thiberge Stephan, Nechushtan Amotz, Sprinzak David, Gileadi Opher, Behar Vered, Zik Ory, Chowers Yehuda, Michaeli Shulamit, Schlessinger Joseph, Moses Elisha
Department of Physics of Complex Systems, The Weizmann Institute of Science, Rehovot 76100, Israel.
Proc Natl Acad Sci U S A. 2004 Mar 9;101(10):3346-51. doi: 10.1073/pnas.0400088101. Epub 2004 Feb 26.
A capability for scanning electron microscopy of wet biological specimens is presented. A membrane that is transparent to electrons protects the fully hydrated sample from the vacuum. The result is a hybrid technique combining the ease of use and ability to see into cells of optical microscopy with the higher resolution of electron microscopy. The resolution of low-contrast materials is approximately 100 nm, whereas in high-contrast materials the resolution can reach 10 nm. Standard immunogold techniques and heavy-metal stains can be applied and viewed in the fluid to improve the contrast. Images present a striking combination of whole-cell morphology with a wealth of internal details. A possibility for direct inspection of tissue slices transpires, imaging only the external layer of cells. Simultaneous imaging with photons excited by the electrons incorporates data on material distribution, indicating a potential for multilabeling and specific scintillating markers.
本文介绍了一种对湿生物标本进行扫描电子显微镜检查的技术。一种对电子透明的膜可保护完全水合的样品免受真空影响。其结果是一种混合技术,它结合了光学显微镜易于使用和能够观察细胞内部的能力以及电子显微镜更高的分辨率。低对比度材料的分辨率约为100纳米,而在高对比度材料中,分辨率可达到10纳米。可以在液体中应用和观察标准免疫金技术和重金属染色剂,以提高对比度。图像呈现出全细胞形态与丰富内部细节的惊人结合。出现了直接检查组织切片的可能性,仅对细胞外层进行成像。利用电子激发的光子进行同步成像可纳入有关材料分布的数据,这表明存在多标记和特定闪烁标记的潜力。