Lütz-Meindl U, Aichinger N
Institute of Plant Physiology, University of Salzburg, Hellbrunnerstrasse 34, 5020 Salzburg, Austria.
Protoplasma. 2004 Jun;223(2-4):155-62. doi: 10.1007/s00709-003-0033-3. Epub 2004 Apr 21.
In the present study energy-filtering transmission electron microscopy by use of an in-column spectrometer is employed as a powerful tool for ultrastructural analysis of plant cells. Images of unstained very thin (50 nm) and thick (140 nm) sections of the unicellular green alga Micrasterias denticulata, as a model system for a growing plant cell, taken by conventional transmission electron microscopy are compared to those obtained from filtering at zero energy loss (elastic bright field) and to those generated by energy filtering below the carbon-specific absorption edge at about 250 eV. The results show that the high-contrast images produced by the latter technique are distinctly superior in contrast and information content to micrographs taken at conventional transmission electron microscopy mode or at elastic bright field. Post- or en bloc staining with heavy metals, which is indispensable for conventional bright-field transmission electron microscopy, can be completely omitted. Delicate structural details such as membranous or filamentous connections between organelles, organelle interactions, or vesicle and vacuole contents are clearly outlined against the cytoplasmic background. Also, immunoelectron microscopic localization of macromolecules benefits from energy-filtering transmission electron microscopy by a better and more accurate assignment of antigens and structures and by facilitating the detection of immunomarkers without renunciation of contrast.
在本研究中,使用柱内光谱仪的能量过滤透射电子显微镜被用作植物细胞超微结构分析的有力工具。将传统透射电子显微镜拍摄的单细胞绿藻齿状微星鼓藻(作为生长中植物细胞的模型系统)未染色的超薄(50纳米)和厚(140纳米)切片的图像,与在零能量损失过滤(弹性明场)下获得的图像以及在约250电子伏特的碳特异性吸收边缘以下进行能量过滤生成的图像进行比较。结果表明,后一种技术产生的高对比度图像在对比度和信息含量方面明显优于在传统透射电子显微镜模式或弹性明场下拍摄的显微照片。传统明场透射电子显微镜不可或缺的重金属后染色或整体染色可以完全省略。细胞器之间的膜状或丝状连接、细胞器相互作用或囊泡和液泡内容物等精细结构细节在细胞质背景下清晰可见。此外,大分子的免疫电子显微镜定位也受益于能量过滤透射电子显微镜,它能更好、更准确地确定抗原和结构,并有助于在不放弃对比度的情况下检测免疫标记物。