Advances in Imaging Secondary Ion Mass Spectrometry for Biological Samples

被引:241
作者
Boxer, Steven G. [1 ]
Kraft, Mary L. [2 ]
Weber, Peter K. [3 ]
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
[2] Univ Illinois, Dept Chem & Biomol Engn, Urbana, IL 61801 USA
[3] Lawrence Livermore Natl Lab, Glenn T Seaborg Inst, Livermore, CA 94551 USA
关键词
membrane organization; chemical composition imaging; NanoSIMS; ToF-SIMS; dynamic SIMS; SUPPORTED LIPID-BILAYERS; SINGLE-CELL LEVEL; TOF-SIMS; FLUORESCENCE MICROSCOPY; CHOLESTEROL DOMAINS; NITROGEN-FIXATION; RESOLUTION; NANOSIMS; TISSUE; MEMBRANES;
D O I
10.1146/annurev.biophys.050708.133634
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Imaging mass spectrometry combines the power of miss spectrometry to identify complex molecules based on mass with simple imaging. Recent advances in secondary ion mass spectrometry have improved sensitivity and spatial resolution, so that these methods have the potential to bridge between high-resolution structures obtained by X-ray crystallography and cyro-electron microscopy and ultrastructure visualized by conventional light microscopy. Following background information on the method and instrumentation, we address the key issue of sample preparation. Because mass spectrometry is performed ill high vacuum, it is essential to preserve the lateral organization of the sample while removing bulk water, and this has been major barrier for applications to biological systems. Recent applications of imaging mass spectrometry to cell biology, microbial communi ties, and biosynthetic pathways are summarized briefly, and studies of biological membrane organization are described in greater depth.
引用
收藏
页码:53 / 74
页数:22
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