Suppr超能文献

人源组织蛋白酶 B 形成淀粉样纤维过程中初始寡聚物的作用

The role of initial oligomers in amyloid fibril formation by human stefin B.

机构信息

Department of Biochemistry, Molecular and Structural Biology, Jožef Stefan Institute, Ljubljana 1000, Slovenia.

出版信息

Int J Mol Sci. 2013 Sep 5;14(9):18362-84. doi: 10.3390/ijms140918362.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b55c/3794784/17498c2e625f/ijms-14-18362f1.jpg

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