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首页> 外文期刊>Journal of Structural Biology >Review: Formation and properties of amyloid-like fibrils derived from alpha-synuclein and related proteins [Review]
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Review: Formation and properties of amyloid-like fibrils derived from alpha-synuclein and related proteins [Review]

机译:综述:α-突触核蛋白和相关蛋白衍生的淀粉样样原纤维的形成和性质[综述]

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摘要

Synucleins are small proteins that are highly expressed in brain tissue and are localised at presynaptic terminals in neurons. alpha-Synuclein has been identified as a component of intracellular fibrillar protein deposits in several neurodegenerative diseases, and two mutant forms of alpha-synuclein have been associated with autosomal-dominant Parkinson's Disease. A fragment of alpha-synuclein has also been identified as the non-A beta component of Alzheimer's Disease amyloid. In this review we describe some structural properties of alpha-synuclein and the two mutant forms, as well as alpha-synuclein fragments, with particular emphasis on their ability to form beta-sheet on ageing and aggregate to form amyloid-like fibrils. Differences in the rates of aggregation and morphologies of the fibrils formed by alpha-synuclein and the two mutant proteins are highlighted. Interactions between alpha-synuclein and other proteins, especially those that are components of amyloid or Lewy bodies, are considered. The toxicity of alpha-synuclein and related peptides towards neurons is also discussing in relation to the aetiology of neurodegenerative diseases. (C) 2000 Academic Press. [References: 52]
机译:突触核蛋白是在脑组织中高度表达的小蛋白,位于神经元的突触前末端。在几种神经退行性疾病中,α-突触核蛋白已被确定为细胞内纤维状蛋白沉积物的组成部分,并且α-突触核蛋白的两种突变形式与常染色体显性帕金森氏病有关。 α-突触核蛋白的片段也已被鉴定为阿尔茨海默氏病淀粉样蛋白的非Aβ成分。在这篇综述中,我们描述了α-突触核蛋白和这两种突变形式以及α-突触核蛋白片段的一些结构特性,特别强调了它们在衰老时形成β-折叠和聚集形成淀粉样蛋白原纤维的能力。突出了由α-突触核蛋白和两种突变蛋白形成的原纤维的聚集速率和形态的差异。考虑了α-突触核蛋白与其他蛋白质之间的相互作用,特别是淀粉样蛋白或路易小体的组成部分之间的相互作用。关于神经退行性疾病的病因,α-突触核蛋白和相关肽对神经元的毒性也在讨论中。 (C)2000学术出版社。 [参考:52]

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