The development and use of metal-based probes for X-ray fluorescence microscopy.
Tiffany W Victor-LovelaceLisa M MillerPublished in: Metallomics : integrated biometal science (2022)
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.
Keyphrases
- high resolution
- single molecule
- dual energy
- single cell
- quantum dots
- cell therapy
- gene expression
- electron microscopy
- living cells
- induced apoptosis
- stem cells
- computed tomography
- high speed
- fluorescent probe
- optical coherence tomography
- high throughput
- label free
- magnetic resonance
- transcription factor
- mass spectrometry
- cell proliferation
- cell death
- amino acid
- fluorescence imaging
- current status