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L723P 家族突变可通过 Ε 裂解位点的局部展开来改变 APP 跨膜结构域替代裂解级联的分布,提示阿尔茨海默病发病机制的一种直接机制。

Familial L723P Mutation Can Shift the Distribution between the Alternative APP Transmembrane Domain Cleavage Cascades by Local Unfolding of the Ε-Cleavage Site Suggesting a Straightforward Mechanism of Alzheimer's Disease Pathogenesis.

机构信息

Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry RAS , Moscow , 117198 , Russian Federation.

Moscow Institute of Physics and Technology , Dolgoprudnyi , 141701 , Russian Federation.

出版信息

ACS Chem Biol. 2019 Jul 19;14(7):1573-1582. doi: 10.1021/acschembio.9b00309. Epub 2019 Jun 19.

Abstract

Alzheimer's disease is an age-related pathology associated with accumulation of amyloid-β peptides, products of enzymatic cleavage of amyloid-β precursor protein (APP) by secretases. Several familial mutations causing early onset of the disease have been identified in the APP transmembrane (TM) domain. The mutations influence production of amyloid-β, but the molecular mechanisms of this effect are unclear. The "Australian" (L723P) mutation located in the C-termini of APP TM domain is associated with autosomal-dominant, early onset Alzheimer's disease. Herein, we describe the impact of familial L723P mutation on the structural-dynamic behavior of APP TM domain studied by high-resolution NMR in membrane-mimicking micelles and augmented by molecular dynamics simulations in explicit lipid bilayer. We found L723P mutation to cause local unfolding of the C-terminal turn of the APP TM domain helix and increase its accessibility to water required for cleavage of the protein backbone by γ-secretase in the ε-site, thus switching between alternative ("pathogenic" and "non-pathogenic") cleavage cascades. These findings suggest a straightforward mechanism of the pathogenesis associated with this mutation, and are of generic import for understanding the molecular-level events associated with APP sequential proteolysis resulting in accumulation of the pathogenic forms of amyloid-β. Moreover, age-related onset of Alzheimer's disease can be explained by a similar mechanism, where the effect of mutation is emulated by the impact of local environmental factors, such as oxidative stress and/or membrane lipid composition. Knowledge of the mechanisms regulating generation of amyloidogenic peptides of different lengths is essential for development of novel treatment strategies of the Alzheimer's disease.

摘要

阿尔茨海默病是一种与淀粉样β肽积累相关的与年龄相关的病理学,淀粉样β肽是淀粉样β前体蛋白(APP)经蛋白酶切割产生的产物。在 APP 跨膜(TM)结构域中已经鉴定出几种导致疾病早发的家族性突变。这些突变影响淀粉样β的产生,但这种效应的分子机制尚不清楚。位于 APP TM 结构域 C 末端的“澳大利亚”(L723P)突变与常染色体显性遗传、早发性阿尔茨海默病有关。在此,我们通过在膜模拟胶束中使用高分辨率 NMR 并通过在明确定义的脂质双层中进行分子动力学模拟来描述家族性 L723P 突变对 APP TM 结构域结构-动力学行为的影响。我们发现 L723P 突变会导致 APP TM 结构域螺旋的 C 末端转角局部展开,并增加其对 γ-分泌酶在 ε 位切割蛋白质骨架所需的水的可及性,从而在替代(“致病性”和“非致病性”)切割级联之间切换。这些发现表明了与该突变相关的发病机制的直接机制,并且对于理解与 APP 顺序蛋白水解相关的分子水平事件以及导致致病性淀粉样β形式积累的通用重要性。此外,阿尔茨海默病的年龄相关性发病可以通过类似的机制来解释,其中突变的影响可以通过局部环境因素(如氧化应激和/或膜脂质组成)的影响来模拟。了解调节不同长度淀粉样肽产生的机制对于开发阿尔茨海默病的新治疗策略至关重要。

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