scholarly journals Tau protein liquid–liquid phase separation can initiate tau aggregation

2018 ◽  
Vol 37 (7) ◽  
Author(s):  
Susanne Wegmann ◽  
Bahareh Eftekharzadeh ◽  
Katharina Tepper ◽  
Katarzyna M Zoltowska ◽  
Rachel E Bennett ◽  
...  
Keyword(s):  
Phase Separation ◽  
Liquid Phase ◽  
Tau Protein ◽  
Liquid Phase Separation ◽  
Tau Aggregation ◽  
Liquid Liquid Phase Separation

scholarly journals Liquid–liquid phase separation of tau protein: The crucial role of electrostatic interactions

2019 ◽  
Vol 294 (29) ◽  
pp. 11054-11059 ◽  
Author(s):  
Solomiia Boyko ◽  
Xu Qi ◽  
Tien-Hao Chen ◽  
Krystyna Surewicz ◽  
Witold K. Surewicz
Keyword(s):  
Phase Separation ◽  
Liquid Phase ◽  
Tau Protein ◽  
Crucial Role ◽  
Electrostatic Interactions ◽  
Liquid Phase Separation ◽  
Liquid Liquid Phase Separation

scholarly journals Liquid-liquid phase separation and fibrillization of tau are independent processes with overlapping conditions

2019 ◽  
Author(s):  
Yanxian Lin ◽  
Yann Fichou ◽  
Zhikai Zeng ◽  
Nicole Y. Hu ◽  
Songi Han
Keyword(s):  
Phase Separation ◽  
Liquid Phase ◽  
Liquid Phase Separation ◽  
Amyloid Aggregation ◽  
Physiological Conditions ◽  
Three Stages ◽  
Tau Aggregation ◽  
Kinetics Of ◽  
Liquid Liquid Phase Separation

AbstractAmyloid aggregation of the microtubule binding protein tau is a hallmark of Alzheimer’s disease and many other neurodegenerative diseases. Recently, tau has been found to undergo liquid-liquid phase separation (LLPS) near physiological conditions. Although LLPS and aggregation have been shown to simultaneously occur under certain common conditions, it remains to be seen whether tau LLPS promotes aggregation, or if they are two independent processes. In this study, we address this question by combining multiple biochemical and biophysical assays in vitro. We investigated the impacts of LLPS on tau aggregation at three stages: conformation of tau, kinetics of aggregation and fibril quantity. We showed that none of these properties are influenced directly by LLPS, while amyloid aggregation propensity of tau can be altered without affecting its LLPS behavior. LLPS and amyloid aggregation of tau occur under overlapping conditions of enhanced intermolecular interactions and localization, but are two independent processes.

scholarly journals Regulatory mechanisms of tau protein fibrillation under the conditions of liquid–liquid phase separation

2020 ◽  
Vol 117 (50) ◽  
pp. 31882-31890
Author(s):  
Solomiia Boyko ◽  
Krystyna Surewicz ◽  
Witold K. Surewicz
Keyword(s):  
Phase Separation ◽  
Liquid Phase ◽  
Tau Protein ◽  
Phenotypic Variability ◽  
Total Concentration ◽  
Liquid Phase Separation ◽  
Liquid Droplets ◽  
Tau Isoforms ◽  
Protein Fibrillation ◽  
Liquid Liquid Phase Separation

One of the hallmarks of Alzheimer’s disease and several other neurodegenerative disorders is the aggregation of tau protein into fibrillar structures. Building on recent reports that tau readily undergoes liquid–liquid phase separation (LLPS), here we explored the relationship between disease-related mutations, LLPS, and tau fibrillation. Our data demonstrate that, in contrast to previous suggestions, pathogenic mutations within the pseudorepeat region do not affect tau441’s propensity to form liquid droplets. LLPS does, however, greatly accelerate formation of fibrillar aggregates, and this effect is especially dramatic for tau441 variants with disease-related mutations. Most important, this study also reveals a previously unrecognized mechanism by which LLPS can regulate the rate of fibrillation in mixtures containing tau isoforms with different aggregation propensities. This regulation results from unique properties of proteins under LLPS conditions, where total concentration of all tau variants in the condensed phase is constant. Therefore, the presence of increasing proportions of the slowly aggregating tau isoform gradually lowers the concentration of the isoform with high aggregation propensity, reducing the rate of its fibrillation. This regulatory mechanism may be of direct relevance to phenotypic variability of tauopathies, as the ratios of fast and slowly aggregating tau isoforms in brain varies substantially in different diseases.

scholarly journals Liquid-liquid phase separation of tau driven by hydrophobic interaction facilitates fibrillization of tau

2020 ◽  
Author(s):  
Yanxian Lin ◽  
Yann Fichou ◽  
Andrew P. Longhini ◽  
Luana C. Llanes ◽  
Yinson Yin ◽  
...  
Keyword(s):  
Phase Separation ◽  
Liquid Phase ◽  
Tau Protein ◽  
Liquid Phase Separation ◽  
Complex Coacervation ◽  
Amyloid Aggregation ◽  
Apparent Conflict ◽  
Liquid Liquid Phase Separation

AbstractAmyloid aggregation of tau protein is implicated in neurodegenerative diseases, yet its facilitating factors are poorly understood. Recently, tau has been shown to undergo liquid liquid phase separation (LLPS) both in vivo and in vitro. LLPS was shown to facilitate tau amyloid aggregation in certain cases, while independent of aggregation in other cases. It is therefore important to understand the differentiating properties that resolve this apparent conflict. We report on a model system of hydrophobically driven LLPS induced by high salt concentration (LLPS-HS), and compare it to electrostatically driven LLPS represented by tau-RNA/heparin complex coacervation (LLPS-ED). We show that LLPS-HS promotes tau protein dehydration, undergoes maturation and directly leads to canonical tau fibrils, while LLPS-ED is reversible, remains hydrated and does not promote amyloid aggregation. We show that the nature of the interaction driving tau condensation is the differentiating factor between aggregation-prone and aggregation-independent LLPS.

Ubiquitination of Alzheimer's-related tau protein affects liquid-liquid phase separation in a site- and cofactor-dependent manner

2022 ◽  
Vol 201 ◽  
pp. 173-181
Author(s):  
Francesca Parolini ◽  
Roberto Tira ◽  
Carlo Giorgio Barracchia ◽  
Francesca Munari ◽  
Stefano Capaldi ◽  
...  
Keyword(s):  
Phase Separation ◽  
Liquid Phase ◽  
Tau Protein ◽  
Liquid Phase Separation ◽  
Dependent Manner ◽  
A Site ◽  
Liquid Liquid Phase Separation

Liquid–Liquid Phase Separation of Tau Protein Is Encoded at the Monomeric Level

2021 ◽  
pp. 2576-2586
Author(s):  
Xuewei Dong ◽  
Santu Bera ◽  
Qin Qiao ◽  
Yiming Tang ◽  
Zenghui Lao ◽  
...  
Keyword(s):  
Phase Separation ◽  
Liquid Phase ◽  
Tau Protein ◽  
Liquid Phase Separation ◽  
Liquid Liquid Phase Separation

scholarly journals Liquid-Liquid Phase Separation of Tau Driven by Hydrophobic Interaction Facilitates Fibrillization of Tau

2021 ◽  
Vol 433 (2) ◽  
pp. 166731
Author(s):  
Yanxian Lin ◽  
Yann Fichou ◽  
Andrew P. Longhini ◽  
Luana C. Llanes ◽  
Pengyi Yin ◽  
...  
Keyword(s):  
Phase Separation ◽  
Liquid Phase ◽  
Hydrophobic Interaction ◽  
Liquid Phase Separation ◽  
Liquid Liquid Phase Separation

scholarly journals Amyloid Aggregation under the Lens of Liquid–Liquid Phase Separation

2020 ◽  
pp. 368-378
Author(s):  
Yanting Xing ◽  
Aparna Nandakumar ◽  
Aleksandr Kakinen ◽  
Yunxiang Sun ◽  
Thomas P. Davis ◽  
...  
Keyword(s):  
Phase Separation ◽  
Liquid Phase ◽  
Liquid Phase Separation ◽  
Amyloid Aggregation ◽  
Liquid Liquid Phase Separation
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