Department of Biochemistry, Molecular and Structural Biology, Jožef Stefan Institute, Ljubljana 1000, Slovenia.
Int J Mol Sci. 2013 Sep 5;14(9):18362-84. doi: 10.3390/ijms140918362.
Oligomers are commonly observed intermediates at the initial stages of amyloid fibril formation. They are toxic to neurons and cause decrease in neural transmission and long-term potentiation. We describe an in vitro study of the initial steps in amyloid fibril formation by human stefin B, which proved to be a good model system. Due to relative stability of the initial oligomers of stefin B, electrospray ionization mass spectrometry (ESI MS) could be applied in addition to size exclusion chromatography (SEC). These two techniques enabled us to separate and detect distinguished oligomers from the monomers: dimers, trimers, tetramers, up to decamers. The amyloid fibril formation process was followed at different pH and temperatures, including such conditions where the process was slow enough to detect the initial oligomeric species at the very beginning of the lag phase and those at the end of the lag phase. Taking into account the results of the lower-order oligomers transformations early in the process, we were able to propose an improved model for the stefin B fibril formation.
寡聚物是淀粉样纤维形成初始阶段常见的中间体。它们对神经元有毒性,导致神经传递和长时程增强减少。我们描述了人源组织蛋白酶 B 淀粉样纤维形成初始步骤的体外研究,结果证明这是一个很好的模型系统。由于组织蛋白酶 B 的初始寡聚物相对稳定,除了尺寸排阻色谱 (SEC) 之外,还可以应用电喷雾电离质谱 (ESI MS)。这两种技术使我们能够从单体中分离和检测到不同的寡聚物:二聚体、三聚体、四聚体,甚至十聚体。在不同的 pH 值和温度下,我们跟踪了淀粉样纤维的形成过程,包括在过程足够缓慢的情况下,在滞后期的起始阶段检测到初始寡聚体,以及在滞后期结束时检测到初始寡聚体的情况。考虑到过程早期低阶寡聚物转化的结果,我们能够提出一个改进的组织蛋白酶 B 纤维形成模型。