Subcellular speciation analysis of trace element oxidation states using synchrotron radiation micro-X-ray absorption near-edge structure

被引:61
作者
Bacquart, Thomas
Deves, Guillaume
Carmona, Asuncion
Tucoulou, Remi
Bohic, Sylvain
Ortega, Richard
机构
[1] Univ Bordeaux 1, CNRS, CNAB UMR 5084, Cellular Chem Imaging & Speciat Grp, F-33175 Gradignan, France
[2] European Synchrotron Radiat Facil, ID Beamline 22, F-38043 Grenoble, France
关键词
D O I
10.1021/ac0711135
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Identification of chemical species at a subcellular level is a key to understand the mechanisms involved in the biology of chemical elements. When performed with a microbeam, X-ray absorption near-edge structure (micro-XANES) enables the direct speciation analysis of oxidation states in subcellular compartments avoiding cell fractionation and other preparation steps that might modify the chemical species. Here we report the principal characteristics in terms of spatial resolution, detection limit, reproducibility, and repeatability of a micro-XANES experimental setup based on Kirkpatrick-Baez X-ray focusing optics that maintains high flux of incoming radiation (> 1011 photons/s) at micromettic spatial resolution (1.5 x 4.0,mu m(2)). Applications and limitations of this setup are illustrated by examples of iron and arsenic absorption spectra obtained from the cytosol, nucleus, and mitochondrial network of cultured cells. A better repeatability and sensitivity with no oxidation state modification and minimal beam damage is achieved when cells are analyzed in a frozen hydrated state, as compared to freeze-dried cells. 'Mis original experimental setup can now be applied for the direct speciation analysis of most trace elements at the subcellular level.
引用
收藏
页码:7353 / 7359
页数:7
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