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dc.contributor.authorJarosova, Romana
dc.contributor.authorWoolfolk, Sarah K.
dc.contributor.authorMartinez-Rivera, Noraida
dc.contributor.authorJaeschke, Mathew W.
dc.contributor.authorRosa-Molinar, Eduardo
dc.contributor.authorTamerler, Candan
dc.contributor.authorJohnson, Michael A.
dc.date.accessioned2023-04-11T19:14:07Z
dc.date.available2023-04-11T19:14:07Z
dc.date.issued2023-02-28
dc.identifier.citationJarosova, R.; Woolfolk, S.K.; Martinez-Rivera, N.; Jaeschke, M.W.; Rosa-Molinar, E.; Tamerler, C.; Johnson, M.A. Spatiotemporal Imaging of Zinc Ions in Zebrafish Live Brain Tissue Enabled by Fluorescent Bionanoprobes. Molecules 2023, 28, 2260. https://doi.org/10.3390/molecules28052260en_US
dc.identifier.urihttps://hdl.handle.net/1808/34095
dc.description.abstractThe 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.en_US
dc.publisherMDPIen_US
dc.rights© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.en_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.subjectZincen_US
dc.subjectGolden_US
dc.subjectNanoparticlesen_US
dc.subjectZebrafishen_US
dc.subjectTwo-photon excitation imagingen_US
dc.subjectFluorescenceen_US
dc.titleSpatiotemporal Imaging of Zinc Ions in Zebrafish Live Brain Tissue Enabled by Fluorescent Bionanoprobesen_US
dc.typeArticleen_US
kusw.kuauthorJarosova, Romana
kusw.kuauthorWoolfolk, Sarah K.
kusw.kuauthorMartinez-Rivera, Noraida
kusw.kuauthorJaeschke, Mathew W.
kusw.kuauthorRosa-Molinar, Eduardo
kusw.kuauthorTamerler, Candan
kusw.kuauthorJohnson, Michael A.
kusw.kudepartmentChemistryen_US
kusw.kudepartmentR.N. Adams Institute for Bioanalytical Chemistryen_US
kusw.kudepartmentInstitute for Bioengineering Researchen_US
kusw.kudepartmentBioengineering Programen_US
kusw.kudepartmentMicroscopy and Analytical Imaging Research Resource Core Laboratoryen_US
kusw.kudepartmentMechanical Engineeringen_US
kusw.kudepartmentPharmacology & Toxicologyen_US
dc.identifier.doi10.3390/molecules28052260en_US
dc.identifier.orcidhttps://orcid.org/0000-0001-6721-4394en_US
dc.identifier.orcidhttps://orcid.org/0000-0003-2057-8937en_US
dc.identifier.orcidhttps://orcid.org/0000-0002-1960-2218en_US
dc.identifier.orcidhttps://orcid.org/0000-0001-5078-9896en_US
kusw.oaversionScholarly/refereed, publisher versionen_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US
dc.identifier.pmidPMC10005619en_US
dc.rights.accessrightsopenAccessen_US


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© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.
Except where otherwise noted, this item's license is described as: © 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.