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淀粉样β肽前体在组成性加工过程中的切割。

Cleavage of amyloid beta peptide during constitutive processing of its precursor.

作者信息

Esch F S, Keim P S, Beattie E C, Blacher R W, Culwell A R, Oltersdorf T, McClure D, Ward P J

机构信息

Athena Neurosciences, Incorporated, South San Francisco, CA 94080.

出版信息

Science. 1990 Jun 1;248(4959):1122-4. doi: 10.1126/science.2111583.

Abstract

The amyloid beta peptide (A beta P) is a small fragment of the much larger, broadly distributed amyloid precursor protein (APP). Abundant A beta P deposition in the brains of patients with Alzheimer's disease suggests that altered APP processing may represent a key pathogenic event. Direct protein structural analyses showed that constitutive processing in human embryonic kidney 293 cells cleaves APP in the interior of the A beta P, thus preventing A beta P deposition. A deficiency of this processing event may ultimately prove to be the etiological event in Alzheimer's disease that gives rise to senile plaque formation.

摘要

淀粉样β肽(AβP)是分布广泛的、更大的淀粉样前体蛋白(APP)的一个小片段。阿尔茨海默病患者大脑中大量的AβP沉积表明,APP加工过程的改变可能是一个关键的致病事件。直接的蛋白质结构分析表明,人胚肾293细胞中的组成性加工在AβP内部切割APP,从而防止AβP沉积。这一加工事件的缺陷最终可能被证明是导致阿尔茨海默病中形成老年斑的病因。

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