Spatiotemporal Imaging of Zinc Ions in Zebrafish Live Brain Tissue Enabled by Fluorescent Bionanoprobes.
Creators
- 1. Department of Chemistry and R.N. Adams Institute for Bioanalytical Chemistry, University of Kansas, Lawrence, KS 66045, USA.
- 2. University of Kansas
- 3. UNESCO Laboratory of Environmental Electrochemistry, Department of Analytical Chemistry, Charles University, 12843 Prague 2, Czech Republic.
- 4. Charles University in Prague
- 5. Institute for Bioengineering Research, University of Kansas, Lawrence, KS 66045, USA.
- 6. Bioengineering Program, University of Kansas, Lawrence, KS 66045, USA.
- 7. Microscopy and Analytical Imaging Research Resource Core Laboratory, University of Kansas, Lawrence, KS 66045, USA.
- 8. Department of Mechanical Engineering, University of Kansas, Lawrence, KS 66045, USA.
- 9. Department of Pharmacology & Toxicology, University of Kansas, Lawrence, KS 66045, USA.
Description
The zebrafish is a powerful model organism to study the mechanisms governing transition metal ions within whole brain tissue. Zinc is one of the most abundant metal ions in the brain, playing a critical pathophysiological role in neurodegenerative diseases. The homeostasis of free, ionic zinc (Zn2+) is a key intersection point in many of these diseases, including Alzheimer's disease and Parkinson's disease. A Zn2+ imbalance can eventuate several disturbances that may lead to the development of neurodegenerative changes. Therefore, compact, reliable approaches that allow the optical detection of Zn2+ across the whole brain would contribute to our current understanding of the mechanisms that underlie neurological disease pathology. We developed an engineered fluorescence protein-based nanoprobe that can spatially and temporally resolve Zn2+ in living zebrafish brain tissue. The self-assembled engineered fluorescence protein on gold nanoparticles was shown to be confined to defined locations within the brain tissue, enabling site specific studies, compared to fluorescent protein-based molecular tools, which diffuse throughout the brain tissue. Two-photon excitation microscopy confirmed the physical and photometrical stability of these nanoprobes in living zebrafish (Danio rerio) brain tissue, while the addition of Zn2+ quenched the nanoprobe fluorescence. Combining orthogonal sensing methods with our engineered nanoprobes will enable the study of imbalances in homeostatic Zn2+ regulation. The proposed bionanoprobe system offers a versatile platform to couple metal ion specific linkers and contribute to the understanding of neurological diseases.
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References
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