The development and use of metal-based probes for X-ray fluorescence microscopy

被引:2
|
作者
Victor-Lovelace, Tiffany W. [1 ]
Miller, Lisa M. [1 ,2 ]
机构
[1] Brookhaven Natl Lab, Natl Synchrotron Light Source 2, Upton, NY 11973 USA
[2] SUNY Stony Brook, Dept Chem, Stony Brook, NY 11794 USA
关键词
X-ray fluorescence imaging; synchrotron; antibody; fluorophore; affinity tag; metal probe; ELECTRON-MICROSCOPY; NANOPROBE BEAMLINE; GOLD NANOPARTICLES; TIO2; NANOPARTICLES; CONTRAST AGENTS; CELLULAR UPTAKE; QUANTUM DOTS; PROTEINS; RESOLUTION; CELLS;
D O I
10.1093/mtomcs/mfac093
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
X-ray fluorescence microscopy (XFM) has become a widely used technique for imaging the concentration and distribution of metal ions in cells and tissues. Recent advances in synchrotron sources, optics, and detectors have improved the spatial resolution of the technique to <10 nm with attogram detection sensitivity. However, to make XFM most beneficial for bioimaging-especially at the nanoscale-the metal ion distribution must be visualized within the subcellular context of the cell. Over the years, a number of approaches have been taken to develop X-ray-sensitive tags that permit the visualization of specific organelles or proteins using XFM. In this review, we examine the types of X-ray fluorophore used, including nanomaterials and metal ions, and the approaches used to incorporate the metal into their target binding site via antibodies, genetically encoded metal-binding peptides, affinity labeling, or cell-specific peptides. We evaluate their advantages and disadvantages, review the scientific findings, and discuss the needs for future development.
引用
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页数:14
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