Suppr超能文献

通过圆二色光谱研究β-淀粉样蛋白构象对金属亲和力和聚集机制的影响。

The effect of Abeta conformation on the metal affinity and aggregation mechanism studied by circular dichroism spectroscopy.

作者信息

Chen Y R, Huang H B, Chyan C L, Shiao M S, Lin T H, Chen Y C

机构信息

Institute of Medical Science, Tzu Chi University, Hualien, Taiwan.

出版信息

J Biochem. 2006 Apr;139(4):733-40. doi: 10.1093/jb/mvj083.

Abstract

The conformational change and associated aggregation of beta amyloid (Abeta) with or without metals is the main cause of Alzheimer's disease (AD). In order to further understand the effects of Abeta and its associated metals on the aggregation mechanism, the influence of Abeta conformation on the metal affinity and aggregation was investigated using circular dichroism (CD) spectroscopy. The Abeta conformation is dependent on pH and trifluoroethanol (TFE). The binding of metals to Abeta was found to be dependent on the Abeta conformation. The aggregation induced by Abeta itself or its associated metals is completely diminished for Abeta in 40% TFE. Only in 5% and 25% TFE can Abeta undergo an alpha-helix to beta-sheet aggregation, which involve a three-state mechanism for the metal-free state, and a two-state transition for the metal-bound state, respectively. The aggregation-inducing activity of metals is in the order, Cu2+ > Fe3+ > or = Al3+ > Zn2+.

摘要

β淀粉样蛋白(Aβ)无论有无金属存在时的构象变化及相关聚集是阿尔茨海默病(AD)的主要病因。为了进一步了解Aβ及其相关金属对聚集机制的影响,使用圆二色性(CD)光谱研究了Aβ构象对金属亲和力和聚集的影响。Aβ构象取决于pH值和三氟乙醇(TFE)。发现金属与Aβ的结合取决于Aβ构象。对于处于40% TFE中的Aβ,由Aβ自身或其相关金属诱导的聚集完全消失。仅在5%和25% TFE中,Aβ可经历从α螺旋到β折叠的聚集,其中无金属状态涉及三态机制,金属结合状态分别涉及两态转变。金属的聚集诱导活性顺序为:Cu2+ > Fe3+ > 或 = Al3+ > Zn2+。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验