Sugiki Toshihiko, Ichikawa Osamu, Miyazawa-Onami Mayumi, Shimada Ichio, Takahashi Hideo
Japan Biological Informatics Consortium (JBiC), Tokyo, Japan.
Methods Mol Biol. 2012;831:19-36. doi: 10.1007/978-1-61779-480-3_2.
Several protein expression systems are available for the preparation of stable isotope-labeled recombinant proteins for NMR studies. Yeast expression systems have several advantages over prokaryotic systems, such as the widely used Escherichia coli expression system. Protein expression using the methylotrophic yeast Pichia pastoris is commonly employed for the preparation of isotope-labeled proteins. Recently, the hemiascomycete yeast Kluyveromyces lactis expression system was reported as being useful for preparing proteins for NMR studies. Since each yeast expression system has different features, their applications have increased in number. In this chapter, we describe procedures for the efficient production of uniformly isotope-labeled proteins using the P. pastoris and the K. lactis yeast expression systems.
有几种蛋白质表达系统可用于制备用于核磁共振(NMR)研究的稳定同位素标记重组蛋白。酵母表达系统相对于原核系统具有几个优势,比如广泛使用的大肠杆菌表达系统。利用甲基营养型酵母毕赤酵母进行蛋白质表达常用于制备同位素标记蛋白。最近,半子囊菌酵母乳酸克鲁维酵母表达系统被报道可用于制备用于NMR研究的蛋白质。由于每种酵母表达系统都有不同的特点,它们的应用数量有所增加。在本章中,我们描述了使用毕赤酵母和乳酸克鲁维酵母表达系统高效生产均匀同位素标记蛋白的方法。