Dammers Christina, Reiss Kerstin, Gremer Lothar, Lecher Justin, Ziehm Tamar, Stoldt Matthias, Schwarten Melanie, Willbold Dieter
Institute of Complex Systems (ICS-6) Structural Biochemistry, Forschungszentrum Jülich, Jülich, Germany.
Institute of Complex Systems (ICS-6) Structural Biochemistry, Forschungszentrum Jülich, Jülich, Germany; Institut für Physikalische Biologie, Heinrich-Heine-Universität Düsseldorf, Düsseldorf, Germany.
Biophys J. 2017 Apr 25;112(8):1621-1633. doi: 10.1016/j.bpj.2017.03.007.
Pyroglutamate-modified amyloid-β (pEAβ) has been described as a relevant Aβ species in Alzheimer's-disease-affected brains, with pEAβ (3-42) as a dominant isoform. Aβ (1-40) and Aβ (1-42) have been well characterized under various solution conditions, including aqueous solutions containing trifluoroethanol (TFE). To characterize structural properties of pEAβ (3-42) possibly underlying its drastically increased aggregation propensity compared to Aβ (1-42), we started our studies in various TFE-water mixtures and found striking differences between the two Aβ species. Soluble pEAβ (3-42) has an increased tendency to form β-sheet-rich structures compared to Aβ (1-42), as indicated by circular dichroism spectroscopy data. Kinetic assays monitored by thioflavin-T show drastically accelerated aggregation leading to large fibrils visualized by electron microscopy of pEAβ (3-42) in contrast to Aβ (1-42). NMR spectroscopy was performed for backbone and side-chain chemical-shift assignments of monomeric pEAβ (3-42) in 40% TFE solution. Although the difference between pEAβ (3-42) and Aβ (1-42) is purely N-terminal, it has a significant impact on the chemical environment of >20% of the total amino acid residues, as revealed by their NMR chemical-shift differences. Freshly dissolved pEAβ (3-42) contains two α-helical regions connected by a flexible linker, whereas the N-terminus remains unstructured. We found that these α-helices act as a transient intermediate to β-sheet and fibril formation of pEAβ (3-42).
焦谷氨酸修饰的淀粉样β蛋白(pEAβ)被认为是阿尔茨海默病受累大脑中一种相关的Aβ物种,其中pEAβ(3 - 42)是主要的异构体。Aβ(1 - 40)和Aβ(1 - 42)在各种溶液条件下,包括含有三氟乙醇(TFE)的水溶液中,已经得到了充分的表征。为了表征pEAβ(3 - 42)的结构特性,其与Aβ(1 - 42)相比聚集倾向大幅增加可能是其潜在原因,我们在各种TFE - 水混合物中开展了研究,发现这两种Aβ物种之间存在显著差异。圆二色光谱数据表明,与Aβ(1 - 42)相比,可溶性pEAβ(3 - 42)形成富含β - 折叠结构的倾向增加。用硫黄素 - T监测的动力学分析表明,与Aβ(1 - 42)相比,pEAβ(3 - 42)的聚集急剧加速,导致通过电子显微镜观察到形成大的纤维。对40% TFE溶液中的单体pEAβ(3 - 42)进行了核磁共振光谱分析,以确定其主链和侧链的化学位移。尽管pEAβ(3 - 42)和Aβ(1 - 42)之间的差异仅在N端,但通过它们的核磁共振化学位移差异揭示,这对超过20%的总氨基酸残基的化学环境有显著影响。新溶解的pEAβ(3 - 42)包含两个由柔性接头连接的α - 螺旋区域,而N端仍无结构。我们发现这些α - 螺旋作为pEAβ(3 - 42)形成β - 折叠和纤维的瞬时中间体。