A New Dynamic in Mass Spectral Imaging of Single Biological Cells

被引:218
作者
Fletcher, John S. [1 ]
Rabbani, Sadia [1 ]
Henderson, Alex [1 ]
Blenkinsopp, Paul [2 ]
Thompson, Steve P. [3 ]
Lockyer, Nicholas P. [1 ]
Vickerman, John C. [1 ]
机构
[1] Univ Manchester, Sch Chem Engn & Analyt Sci, Manchester Interdisciplinary Bioctr, Manchester, Lancs, England
[2] Ionoptika Ltd, Southampton, Hants, England
[3] Sci Anal Instruments, Manchester, Lancs, England
基金
英国工程与自然科学研究理事会;
关键词
D O I
10.1021/ac8015278
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Time-of-flight secondary ion mass spectrometry (TOF-SIMS) has unique capabilities in the area of high-resolution mass spectrometric imaging of biological samples. The technique offers parallel detection of native and nonnative molecules at physiological concentrations with potentially submicrometer spatial resolution. Recent advances in SIMS technology have been focused on generating new ion sources that can in turn be used to eject more intact molecular and biological characteristic species from a sample. The introduction of polyatomic ion beams, particularly C-60, for TOF-SIMS analysis has created a whole new application of molecular depth profiling and 3D molecular imaging. However, such analyses, particularly at high lateral resolution, are severely hampered by the accompanying mass spectrometry associated with current TOF-SIMS instruments. Hence, we have developed an instrument that overcomes many of the drawbacks of current TOF-SIMS spectrometers by removing the need to pulse the primary ion beam. The instrument samples the secondary ions using a buncher that feeds into a specially designed time-of-flight analyzer. We have validated this new instrumental concept by analyzing a number of biological samples generating 2D and 3D images showing molecular localization on a subcellular scale, over a practical time frame, while maintaining high mass resolution. We also demonstrate large area mapping and the MS/MS capability of the instrument.
引用
收藏
页码:9058 / 9064
页数:7
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