Hydrophobic tagging-mediated degradation of Alzheimer's disease related Tau
Open accessAbstract
HyT-Tau-CPP reduced Tau levels in Alzheimer's disease (AD) mouse model, and appeared to be a promising candidate for AD treatment.
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Exchanging the HALO reactive linker for the Tau-interacting peptide (C-terminal region of tubulin) induced efficient degradation of Tau.
“In an attempt to make the system more applicable and remove the need to create HALO-fusions, the HALO reactive linker was exchanged for the Alzheimer’s disease-related protein Tau-interacting peptide (the C-terminal region of tubulin). This induced efficient degradation of Tau [60].”
From Advances in targeted degradation of endogenous proteins (2019) · cites this paper as [60]
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References 41 · Cited by 62
- Authors
- Gao, N., Chu, T.-T., Li, Q.-Q., Lim, Y.-J., Qiu, T., Ma, M.-R., Hu, Z.-W., Yang, X.-F., Chen, Y.-X., Zhao, Y.-F., & Li, Y.-M.
- Affiliations
- Tsinghua University (CN)
- Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education)
- Key Laboratory of Modern Toxicology of Shenzhen
- Corresponding author
- Chen, Yong-Xiang
- Venue
- RSC Advances
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 2017
- Volume
- 7
- Issue
- 64
- Pages
- 40362-40366
- ISSN
- 2046-2069 (ISSN-L)
- OpenAlex
- W2748160025
- Cited by
- 62
- References
- 41
- Citations by year
- 2026: 7 · 2025: 8 · 2024: 10 · 2023: 10 · 2022: 8 · 2021: 7 · 2020: 5 · 2019: 5 · 2018: 2
- FWCI
- 2.43
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- RSC Advances (publishedVersion, cc-by-nc)
- Topics
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Pharmacology › Cholinesterase and Neurodegenerative Diseases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Interference and Gene Delivery
- Keywords
- tau protein, Alzheimer's disease, protein degradation, tau aggregation, mouse models of Alzheimer's disease, drug candidates
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