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Hybrid Amyloid Quantum Dot Nano-Bio Assemblies to Probe Neuroinflammatory Damage


Journal article


Wesley Chiang, J. Urban, Francine Yanchik-Slade, Angela Stout, Jennetta M Hammond, Bradley L. Nilsson, Harris A Gelbard, Todd D. Krauss
ACS Chemical Neuroscience, 2024

Semantic Scholar DOI PubMedCentral PubMed
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APA   Click to copy
Chiang, W., Urban, J., Yanchik-Slade, F., Stout, A., Hammond, J. M., Nilsson, B. L., … Krauss, T. D. (2024). Hybrid Amyloid Quantum Dot Nano-Bio Assemblies to Probe Neuroinflammatory Damage. ACS Chemical Neuroscience.


Chicago/Turabian   Click to copy
Chiang, Wesley, J. Urban, Francine Yanchik-Slade, Angela Stout, Jennetta M Hammond, Bradley L. Nilsson, Harris A Gelbard, and Todd D. Krauss. “Hybrid Amyloid Quantum Dot Nano-Bio Assemblies to Probe Neuroinflammatory Damage.” ACS Chemical Neuroscience (2024).


MLA   Click to copy
Chiang, Wesley, et al. “Hybrid Amyloid Quantum Dot Nano-Bio Assemblies to Probe Neuroinflammatory Damage.” ACS Chemical Neuroscience, 2024.


BibTeX   Click to copy

@article{wesley2024a,
  title = {Hybrid Amyloid Quantum Dot Nano-Bio Assemblies to Probe Neuroinflammatory Damage},
  year = {2024},
  journal = {ACS Chemical Neuroscience},
  author = {Chiang, Wesley and Urban, J. and Yanchik-Slade, Francine and Stout, Angela and Hammond, Jennetta M and Nilsson, Bradley L. and Gelbard, Harris A and Krauss, Todd D.}
}

Abstract

Various oligomeric species of amyloid-beta have been proposed to play different immunogenic roles in the cellular pathology of Alzheimer’s Disease. The dynamic interconversion between various amyloid oligomers and fibrillar assemblies makes it difficult to elucidate the role each potential aggregation state may play in driving neuroinflammatory and neurodegenerative pathology. The ability to identify the amyloid species that are key and essential drivers of these pathological hallmarks of Alzheimer’s Disease is of fundamental importance for also understanding downstream events including tauopathies that mediate neuroinflammation with neurologic deficits. Here, we report the design and construction of a quantum dot mimetic for larger spherical oligomeric amyloid species as an “endogenously” fluorescent proxy for this cytotoxic assembly of amyloid to investigate its role in inducing inflammatory and stress response states in neuronal and glial cell types. The design parameters and construction protocol developed here may be adapted for developing quantum dot nano-bio assemblies for other biological systems of interest, particularly neurodegenerative diseases involving other protein aggregates.


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