Three-dimensional mass spectral imaging of HeLa-M cells - sample preparation, data interpretation and visualisation

被引:101
作者
Fletcher, John S. [1 ]
Rabbani, Sadia [1 ]
Henderson, Alex [1 ]
Lockyer, Nicholas P. [1 ]
Vickerman, John C. [1 ]
机构
[1] Univ Manchester, Sch Chem Engn & Analyt Sci, Manchester Interdisciplinary Bioctr, Manchester M1 7DN, Lancs, England
基金
英国工程与自然科学研究理事会;
关键词
PRIMARY ION-BEAM; TOF-SIMS ANALYSIS; SPECTROMETRY ANALYSIS; CHEMICAL-COMPOSITION; SINGLE CELLS; ANIMAL-CELLS; BOMBARDMENT; C-60; ENHANCEMENT; SECTIONS;
D O I
10.1002/rcm.4944
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Time-of-flight secondary ion mass spectrometry (ToFSIMS) is being applied increasingly to the study of biological systems where the chemical specificity of mass spectrometry and the high lateral resolution imaging capabilities can be exploited. Here we report a comparison of two cell sample preparation methods and demonstrate how they influence the outcome of the ToFSIMS analysis for three-dimensional (3D) imaging of biological cells using our novel buncher-ToF instrument (J105 3D Chemical Imager) equipped with a C(60) primary ion beam. Cells were analysed fixed and freeze-dried and non-fixed, frozen-hydrated. It is concluded that maintaining the cells in a non-fixed frozen-hydrated state during the analysis helps reduce chemical redistribution, producing cleaner spectra and improved chemical contrast in both 2D and 3D imaging. Insights into data interpretation are included and we present methods for 3D reconstruction of the data using multivariate analysis techniques. Copyright (C) 2011 John Wiley & Sons, Ltd.
引用
收藏
页码:925 / 932
页数:8
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