Trace element mapping of a single cell using a hard x-ray nanobeam focused by a Kirkpatrick-Baez mirror system

被引:46
作者
Matsuyama, S. [1 ]
Shimura, M. [2 ]
Mirnura, H. [1 ]
Fujii, M. [1 ]
Yumoto, H. [3 ]
Sano, Y. [1 ]
Yabashi, M. [3 ]
Nishino, Y. [4 ]
Tamasaku, K. [4 ]
Ishikawa, T. [4 ]
Yamauchi, K. [1 ,5 ]
机构
[1] Osaka Univ, Dept Precis Sci & Technol, Grad Sch Engn, Suita, Osaka 5650871, Japan
[2] Int Med Ctr Japan, Dept Intractable Dis, Shinjuku Ku, Tokyo 1628655, Japan
[3] Spring 8 Synchrotron Radiat Res Inst JASRI, Sayo, Hyogo 6795148, Japan
[4] Spring 8 Riken, Sayo, Hyogo 6795148, Japan
[5] Osaka Univ, Res Ctr Ultra Precis Sci & Technol, Grad Sch Engn, Suita, Osaka 5650871, Japan
关键词
CIS-DIAMMINEDICHLORO-PLATINUM(II); LOCALIZATION; MICROSCOPY;
D O I
10.1002/xrs.1123
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
To visualize the distributions of trace elements in biological samples such as tissues and cells at high spatial resolution, we developed a scanning x-ray fluorescence microscope (SXFM) at SPring-8, using a Kirkpatrick-Baez mirror optics that enables achromatic and highly efficient focusing. To evaluate performance regarding its application to biological samples, the SXFM was used at x-ray energy of 15 keV to observe NIH/3T3 cells in which adenosine triphosphate (ATP) synthase beta (specifically localized at the mitochondria) were labeled with gold colloidal particles. Various elemental distributions were visualized at the single-cell level, including those for P, S, Cl, Ca, Fe, Cu, Zn and Au, and we obtained high-resolution elemental distribution maps by magnifying the labeled single mitochondrion. Maximum spatial resolution achieved in the experiments was sub-100 nm. Copyright (C) 2008 John Wiley & Sons, Ltd.
引用
收藏
页码:89 / 94
页数:6
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