Subcellular mass determination by 4He+ energy-loss micro-spectrometry

被引:13
作者
Devès, G [1 ]
Ortega, R [1 ]
机构
[1] Univ Bordeaux 1, CNRS, UMRS084, F-33175 Gradignan, France
关键词
chemical imaging; scanning transmission ion microscopy; cellular mass; microanalysis; ion-beam analysis;
D O I
10.1007/s00216-002-1511-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The scanning transmission ion microscope (STIM) has been used to determine the intracellular mass of human cultured cells. A He-4(+) microbeam of 2.0 MeV energy was chosen to obtain enhanced ion-energy-loss sensitivity through the micron-thick freeze-dried cells. Local sample mass calculation, based on energy-loss conversion by use of appropriate matrix stopping powers, was performed by use of dedicated software. The method was validated with epoxy resin sections and polymer foil as analogues of biological samples in the range of (intra)cellular thickness, 150 to 3000 nm. STIM analysis resulted in less than 5% error in mass determination. He-4(+) energy-loss micro-spectrometry was performed on freeze-dried human ovarian cancer cells, the mean areal mass obtained was 120 mug cm(-2) (200 mug cm(-2) in the nucleus and 250 mug cm(-2) in nucleoli). This method is particularly useful for mass normalization of X-ray fluorescence yields resulting from particle-induced X-ray emission micro-analysis (micro-PIXE). When performed successively these two ion-beam micro-analytical methods enable the mapping of true element concentrations within single cells.
引用
收藏
页码:390 / 394
页数:5
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