首页> 外文期刊>Journal of Molecular Biology >ACETYLCHOLINESTERASE PROMOTES THE AGGREGATION OF AMYLOID-BETA-PEPTIDE FRAGMENTS BY FORMING A COMPLEX WITH THE GROWING FIBRILS
【24h】

ACETYLCHOLINESTERASE PROMOTES THE AGGREGATION OF AMYLOID-BETA-PEPTIDE FRAGMENTS BY FORMING A COMPLEX WITH THE GROWING FIBRILS

机译:乙酰胆碱酯酶通过与生长中的纤维形成复合物来促进淀粉样蛋白肽片段的聚集

获取原文
获取原文并翻译 | 示例
           

摘要

Acetylcholinesterase (AChE), an enzyme involved in the hydrolysis of the neurotransmitter acetylcholine, consistently colocalizes with the amyloid deposits characteristic of Alzheimer's disease and may contribute to the generation of amyloid proteins and/or physically affect fibril assembly. Ln order to identify the structural domains of the amyloid-beta-peptide (A beta) involved in the aggregation induced by AChE, we have studied the effect of this cholinergic enzyme on A beta peptide fragments of different sizes. AChE enhanced the aggregation of the A beta(12-28) and A beta(25-35) peptides but not of the A beta(1-16) fragment. The inductive effect of AChE on the aggregation of A beta(12-28) was abolished by the presence of either A beta(1-16) or A beta(9-21). The effect of the enzyme was also analysed using two different mutant fragments, possessing a low and the other a high capacity for fibrillogenesis. The fragments used were A beta(12-28)(Val18-->Ala) and A beta(12-28)(Glu22-->Gln), respectively. AChE was able to promote the aggregation of these fragments in a very specific way and both mutant peptides were able to form amyloid fibrils, as revealed by negative staining under the electron microscope. Binding assays indicated that AChE was bound to A beta(12-28), as well as to the A beta(1-16) peptide. AChE was seen to form strong complexes with the A beta(12-28) fibrils as such complexes stained positively for both thioflavine-T and AChE activity, were resistant to high ionic strength treatment, and were partially sensitive to detergents, suggesting that hydrophobic interactions may play a role in the stabilization of the AChE-A beta complex. Our results suggest that such amyloid-AChE complexes are formed when AChE interacts with the growing amyloid fibrils and accelerates the assembly of A beta peptides. This is consistent with the fact that AChE is known to be present within A beta deposits including the pre-amyloid diffuse and mature senile plaques found in Alzheimer's brain. (C) 1997 Academic Press Limited. [References: 62]
机译:乙酰胆碱酯酶(AChE)是一种参与神经递质乙酰胆碱水解的酶,始终与阿尔茨海默氏病特征性淀粉样沉积物共定位,并可能有助于淀粉样蛋白的生成和/或对原纤维的组装产生物理影响。为了鉴定参与AChE诱导的聚集的淀粉样β肽(A beta)的结构域,我们研究了这种胆碱能酶对不同大小的A beta肽片段的影响。 AChE增强了A beta(12-28)和A beta(25-35)肽的聚集,但没有增强A beta(1-16)片段的聚集。 ACh(1-16)或Abeta(9-21)的存在消除了AChE对A beta(12-28)聚集的诱导作用。还使用两个不同的突变片段分析了该酶的作用,这些片段具有较低的原纤维形成能力,而另一个具有较高的原纤维形成能力。使用的片段分别是A beta(12-28)(Val18-> Ala)和A beta(12-28)(Glu22-> Gln)。 AChE能够以非常特定的方式促进这些片段的聚集,并且两种突变体肽都能够形成淀粉样蛋白原纤维,这在电子显微镜下可以看出。结合测定表明,AChE与A beta(12-28)以及A beta(1-16)肽结合。可以看到AChE与A beta(12-28)的原纤维形成了牢固的复合物,因为这种复合物对thioflavine-T和AChE活性均呈阳性染色,对高离子强度处理有抵抗力,并且对去污剂部分敏感,表明疏水性相互作用可能在AChE-A beta复合物的稳定中发挥作用。我们的结果表明,当AChE与生长中的淀粉样蛋白原纤维相互作用并加速Aβ肽的组装时,就会形成此类淀粉样蛋白AChE复合物。这与以下事实相符:已知AChE存在于Aβ沉积物中,包括在阿尔茨海默氏症大脑中发现的淀粉样前弥散性和成熟的老年斑。 (C)1997 Academic Press Limited。 [参考:62]

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号