Department of Biology & Biochemistry, University of Bath, Claverton Down, Bath, BA2 7AY, UK.
Division of Chemistry and Structural Biology, Australian Research Council Centre of Excellence in Advanced Molecular Imaging, Institute for Molecular Bioscience, The University of Queensland, Brisbane, Queensland, 4072, Australia.
Mol Neurodegener. 2019 Jul 22;14(1):29. doi: 10.1186/s13024-019-0329-1.
Alpha-synuclein (αS) is the major constituent of Lewy bodies and a pathogenic hallmark of all synucleinopathathies, including Parkinson's disease (PD), dementia with Lewy bodies (DLB), and multiple system atrophy (MSA). All diseases are determined by αS aggregate deposition but can be separated into distinct pathological phenotypes and diagnostic criteria. Here we attempt to reinterpret the literature, particularly in terms of how αS structure may relate to pathology. We do so in the context of a rapidly evolving field, taking into account newly revealed structural information on both native and pathogenic forms of the αS protein, including recent solid state NMR and cryoEM fibril structures. We discuss how these new findings impact on current understanding of αS and PD, and where this information may direct the field.
α-突触核蛋白(αS)是路易体的主要成分,也是所有突触核蛋白病的致病标志,包括帕金森病(PD)、路易体痴呆(DLB)和多系统萎缩(MSA)。所有疾病都由αS 聚集物沉积决定,但可以分为不同的病理表型和诊断标准。在这里,我们试图重新解释文献,特别是αS 结构如何与病理学相关。我们在一个快速发展的领域中这样做,考虑到αS 蛋白的天然和致病形式的新揭示的结构信息,包括最近的固态 NMR 和 cryoEM 纤维结构。我们讨论了这些新发现如何影响对αS 和 PD 的现有理解,以及这些信息可能在何处指导该领域。