Spahn Claudia, Wermann Michael, Eichentopf Rico, Hause Gerd, Schlenzig Dagmar, Schilling Stephan
Fraunhofer Institute for Cell Therapy and Immunology, Department for Drug Design and Target Validation (IZI-MWT), Halle, Germany.
Martin-Luther University Halle-Wittenberg, Halle, Germany.
Electrophoresis. 2017 Aug;38(16):2042-2049. doi: 10.1002/elps.201700154. Epub 2017 Jun 8.
Recombinant expression and purification of amyloid peptides represents a common basis for investigating the molecular mechanisms of amyloid formation and toxicity. However, the isolation of the recombinant peptides is hampered by inefficient separation from contaminants such as the fusion protein required for efficient expression in E. coli. Here, we present a new approach for the isolation of highly purified Aβ(1-42) and pGlu-Aβ(3-42), which is based on a separation using preparative SDS-PAGE. The method relies on the purification of the Aβ fusion protein by affinity chromatography followed by preparative SDS-PAGE under reducing conditions and subsequent removal of detergents by precipitation. The application of preparative SDS-PAGE represents the key step to isolate highly pure recombinant Aβ, which has been applied for characterization of aggregation and toxicity. Thereby, the yield of the purification strategy was >60%. To the best of our knowledge, this is the first description of an electrophoresis-based method for purification of a recombinant Aβ peptide. Therefore, the method might be of interest for isolation of other amyloid peptides, which are critical for conventional purification strategies due to their aggregation propensity.
淀粉样肽的重组表达和纯化是研究淀粉样蛋白形成和毒性分子机制的共同基础。然而,重组肽的分离受到与污染物(如在大肠杆菌中高效表达所需的融合蛋白)分离效率低下的阻碍。在此,我们提出了一种分离高度纯化的Aβ(1-42)和pGlu-Aβ(3-42)的新方法,该方法基于制备性SDS-PAGE分离。该方法依赖于通过亲和色谱法纯化Aβ融合蛋白,然后在还原条件下进行制备性SDS-PAGE,并随后通过沉淀去除去污剂。制备性SDS-PAGE的应用是分离高度纯合重组Aβ的关键步骤,该重组Aβ已用于聚集和毒性的表征。因此,纯化策略的产率>60%。据我们所知,这是首次描述基于电泳的重组Aβ肽纯化方法。因此,该方法可能对分离其他淀粉样肽感兴趣,这些肽由于其聚集倾向而对传统纯化策略至关重要。