Department of Pharmaceutical Biotechnology, Faculty of Pharmacy, Isfahan University of Medical Sciences, Isfahan, Iran.
Methods Mol Biol. 2023;2617:155-164. doi: 10.1007/978-1-0716-2930-7_10.
Overexpression of heterologous protein in prokaryotic host cells, such as Escherichia coli, usually leads to formation of inactive and insoluble aggregates known as inclusion bodies (IBs). Recovery of refolded and functionally bioactive proteins from IBs is a challenging task, and a unique condition (e.g., solubilizing and refolding buffers) for each individual protein should be experimentally obtained. Here, we present a simple protocol for development of solubilizing and refolding buffers for successful recovery of pure bioactive proteins from IBs.
在原核宿主细胞(如大肠杆菌)中过表达异源蛋白通常会导致形成无活性和不溶性的聚集体,称为包涵体(IBs)。从 IBs 中回收重折叠和功能生物活性的蛋白质是一项具有挑战性的任务,并且应该通过实验获得每种蛋白质的独特条件(例如,溶解和重折叠缓冲液)。在这里,我们提出了一种简单的方案,用于开发溶解和重折叠缓冲液,以成功地从 IBs 中回收纯生物活性蛋白质。