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(−)-Epigallocatechin-3-gallate, a Polyphenol from Green Tea, Regulates the Liquid–Liquid Phase Separation of Alzheimer’s-Related Protein Tau

The microtubule-associated protein tau is involved in Alzheimer’s disease and other tauopathies. Recently, tau has been shown to undergo liquid–liquid phase separation (LLPS), which is implicated in the physiological function and pathological aggregation of tau. In this report, we demonstrate that t...

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Published in:Journal of agricultural and food chemistry 2023-02, Vol.71 (4), p.1982-1993
Main Authors: Chen, Jingxin, Ma, Wanyao, Yu, Jiangchuan, Wang, Xi, Qian, Hongling, Li, Ping, Ye, Haiqiong, Han, Yue, Su, Zhengding, Gao, Meng, Huang, Yongqi
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cited_by cdi_FETCH-LOGICAL-a266t-c1f517a804e87a46b1639b764bb492b29af60a7e6337615cbf2ca6eaf8a2b1d13
cites cdi_FETCH-LOGICAL-a266t-c1f517a804e87a46b1639b764bb492b29af60a7e6337615cbf2ca6eaf8a2b1d13
container_end_page 1993
container_issue 4
container_start_page 1982
container_title Journal of agricultural and food chemistry
container_volume 71
creator Chen, Jingxin
Ma, Wanyao
Yu, Jiangchuan
Wang, Xi
Qian, Hongling
Li, Ping
Ye, Haiqiong
Han, Yue
Su, Zhengding
Gao, Meng
Huang, Yongqi
description The microtubule-associated protein tau is involved in Alzheimer’s disease and other tauopathies. Recently, tau has been shown to undergo liquid–liquid phase separation (LLPS), which is implicated in the physiological function and pathological aggregation of tau. In this report, we demonstrate that the green tea polyphenol (−)-epigallocatechin-3-gallate (EGCG) promotes the formation of liquid tau droplets at neutral pH by creating a network of hydrophobic interactions and hydrogen bonds, mainly with the proline-rich domain of tau. We further show that EGCG oxidation, tau phosphorylation, and the chemical structure of the polyphenol influence the efficacy of EGCG in facilitating tau LLPS. Complementary to the inhibitory activity of EGCG in tau fibrillization, our findings provide novel insights into the biological activity of EGCG and offer new clues for future studies on the molecular mechanism by which EGCG alleviates neurodegenerative diseases.
doi_str_mv 10.1021/acs.jafc.2c07799
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source American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)
subjects Alzheimer Disease - drug therapy
Alzheimer Disease - metabolism
Bioactive Constituents, Metabolites, and Functions
Catechin - chemistry
Humans
Polyphenols
tau Proteins - metabolism
Tea - chemistry
title (−)-Epigallocatechin-3-gallate, a Polyphenol from Green Tea, Regulates the Liquid–Liquid Phase Separation of Alzheimer’s-Related Protein Tau
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