Institut de Biologie et Chimie des Protéines, UMR 5086 CNRS/Université de Lyon 1, 7 passage du Vercors, 69367 Lyon, France.
N Biotechnol. 2011 Apr 30;28(3):232-8. doi: 10.1016/j.nbt.2010.06.016. Epub 2010 Jul 4.
The expression of soluble, functional protein on a preparative scale poses a central challenge for structural studies. Cell-free protein expression has become a valuable alternative to cell-based methods, and allows today the expression of milligram quantities of protein. Its use is particularly attractive for NMR studies as it allows a multitude of isotopic labeling schemes. We have implemented and further developed protocols to prepare cell-free extracts from wheat germ to produce recombinant protein for solid-state NMR studies. Furthermore, we established the Renilla luciferase model to optimise and evaluate extract quality, and report first productions of the prions Ure2p and HET-s devoted to structural studies currently ongoing in our laboratories.
在制备规模上表达可溶性、有功能的蛋白质是结构研究的核心挑战。无细胞蛋白质表达已经成为基于细胞方法的一种有价值的替代方法,并且今天可以表达毫克数量的蛋白质。它特别适用于 NMR 研究,因为它允许多种同位素标记方案。我们已经实施并进一步开发了从小麦胚芽中制备无细胞提取物的方案,以生产用于固态 NMR 研究的重组蛋白。此外,我们建立了海肾荧光素酶模型来优化和评估提取物的质量,并报告了正在我们实验室进行的结构研究中首次生产的 Ure2p 和 HET-s 朊病毒。