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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 |
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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 |
format | article |
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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.</description><identifier>ISSN: 0021-8561</identifier><identifier>EISSN: 1520-5118</identifier><identifier>DOI: 10.1021/acs.jafc.2c07799</identifier><identifier>PMID: 36688583</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Alzheimer Disease - drug therapy ; Alzheimer Disease - metabolism ; Bioactive Constituents, Metabolites, and Functions ; Catechin - chemistry ; Humans ; Polyphenols ; tau Proteins - metabolism ; Tea - chemistry</subject><ispartof>Journal of agricultural and food chemistry, 2023-02, Vol.71 (4), p.1982-1993</ispartof><rights>2023 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a266t-c1f517a804e87a46b1639b764bb492b29af60a7e6337615cbf2ca6eaf8a2b1d13</citedby><cites>FETCH-LOGICAL-a266t-c1f517a804e87a46b1639b764bb492b29af60a7e6337615cbf2ca6eaf8a2b1d13</cites><orcidid>0000-0002-9463-8325 ; 0000-0003-3558-001X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36688583$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Jingxin</creatorcontrib><creatorcontrib>Ma, Wanyao</creatorcontrib><creatorcontrib>Yu, Jiangchuan</creatorcontrib><creatorcontrib>Wang, Xi</creatorcontrib><creatorcontrib>Qian, Hongling</creatorcontrib><creatorcontrib>Li, Ping</creatorcontrib><creatorcontrib>Ye, Haiqiong</creatorcontrib><creatorcontrib>Han, Yue</creatorcontrib><creatorcontrib>Su, Zhengding</creatorcontrib><creatorcontrib>Gao, Meng</creatorcontrib><creatorcontrib>Huang, Yongqi</creatorcontrib><title>(−)-Epigallocatechin-3-gallate, a Polyphenol from Green Tea, Regulates the Liquid–Liquid Phase Separation of Alzheimer’s-Related Protein Tau</title><title>Journal of agricultural and food chemistry</title><addtitle>J. Agric. Food Chem</addtitle><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. 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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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