New versatile staining reagents for biological transmission electron microscopy that substitute for uranyl acetate

被引:78
作者
Nakakoshi, Masamichi [1 ]
Nishioka, Hideo [2 ]
Katayama, Eisaku [1 ]
机构
[1] Univ Tokyo, Inst Med Sci, Div Biomol Imaging, Minato Ku, Tokyo 1088639, Japan
[2] JEOL Ltd, Applicat Grp, EM Business Unit, Tokyo 1968556, Japan
来源
JOURNAL OF ELECTRON MICROSCOPY | 2011年 / 60卷 / 06期
基金
日本科学技术振兴机构;
关键词
transmission electron microscopy; staining reagent; negative staining; uranyl acetate substitute; samarium triacetate; gadolinium triacetate; MOLECULAR-STRUCTURE; TISSUE SECTIONS; LEAD; PH;
D O I
10.1093/jmicro/dfr084
中图分类号
TH742 [显微镜];
学科分类号
摘要
Aqueous uranyl acetate has been extensively used as a superb staining reagent for transmission electron microscopy of biological materials. However, recent regulation of nuclear fuel material severely restricts its use even for purely scientific purposes. Since uranyl salts are hazardous due to biological toxicity and remaining radioactivity, development of safe and non-radioactive substitutes is greatly anticipated. We examined two lanthanide salts, samarium triacetate and gadolinium triacetate, and found that 1-10% solution of these reagents was safe but still possess excellent capability for staining thin sections of plastic-embedded materials of animal and plant origin. Although post-fixation with osmium tetroxide was essential for high-contrast staining, post-staining with lead citrate could be eliminated if a slow-scan CCD camera is available for observation. These lanthanide salts can also be utilized as good negative-staining reagents to study supramolecular architecture of biological macromolecules. They were not as effective as a fixative of protein assembly, reflecting the non-hazardous nature of the reagents.
引用
收藏
页码:401 / 407
页数:7
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