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Tau蛋白与α-突触核蛋白的液-液相分离:治疗神经退行性疾病共病的新靶点。

Liquid-liquid phase separation of Tau and α-synuclein: a new target for treating comorbidity in neurodegeneration.

作者信息

Foressi Nahuel N, Rodríguez Leandro Cruz, Celej M Soledad

机构信息

Departamento de Química Biológica Ranwel Caputto, Centro de Investigaciones en Química Biológica de Córdoba (CIQUIBIC, CONICET), Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, Haya de La Torre y Medina Allende, Ciudad Universitaria, X5000HUA Córdoba, Argentina.

出版信息

Biophys Rev. 2024 Dec 2;17(2):491-498. doi: 10.1007/s12551-024-01259-6. eCollection 2025 Apr.

Abstract

Alzheimer's and Parkinson's diseases are the most common neurodegenerative disorders, causing significant disability and mortality worldwide. Though traditionally classified as Tau and α-synuclein-related disorders, respectively, there is growing evidence of clinical overlap between dementia and Parkinsonism, with comorbidity worsening cognitive impairment and prognosis. Emerging research on liquid-liquid phase separation (LLPS) offers promising insights into novel treatments of these proteinopathies by targeting the phase behavior of the disease-associated proteins. Thus, manipulating condensates has become a focus for developing new therapeutic compounds, termed condensate-modifying drugs (c-mods), by which historically considered undruggable proteins can be targeted. This review offers an overview of bioactive molecules that act as modifiers of Tau and α-synuclein condensates through various mechanisms. The goal is to lay the groundwork for discovering new therapeutic approaches to prevent harmful protein aggregation and treat comorbidity in tau and synucleinopathies.

摘要

阿尔茨海默病和帕金森病是最常见的神经退行性疾病,在全球范围内导致严重的残疾和死亡。尽管传统上分别归类为与 Tau 蛋白和α-突触核蛋白相关的疾病,但越来越多的证据表明痴呆症和帕金森综合征在临床上存在重叠,合并症会加重认知障碍和预后。关于液-液相分离(LLPS)的新兴研究通过针对疾病相关蛋白的相行为,为这些蛋白质病的新治疗方法提供了有前景的见解。因此,操纵凝聚物已成为开发新型治疗化合物(称为凝聚物修饰药物,c-mods)的重点,通过这种方法可以靶向历史上被认为不可成药的蛋白质。本综述概述了通过各种机制作为 Tau 蛋白和α-突触核蛋白凝聚物修饰剂的生物活性分子。目的是为发现预防有害蛋白质聚集和治疗 Tau 蛋白病和突触核蛋白病合并症的新治疗方法奠定基础。

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本文引用的文献

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