Sitarska Agnieszka, Skora Lukasz, Klopp Julia, Roest Susan, Fernández César, Shrestha Binesh, Gossert Alvar D
Novartis Institutes for BioMedical Research, 4002, Basel, Switzerland.
J Biomol NMR. 2015 Jun;62(2):191-7. doi: 10.1007/s10858-015-9935-6. Epub 2015 May 1.
For a wide range of proteins of high interest, the major obstacle for NMR studies is the lack of an affordable eukaryotic expression system for isotope labeling. Here, a simple and affordable protocol is presented to produce uniform labeled proteins in the most prevalent eukaryotic expression system for structural biology, namely Spodoptera frugiperda insect cells. Incorporation levels of 80% can be achieved for (15)N and (13)C with yields comparable to expression in full media. For (2)H,(15)N and (2)H,(13)C,(15)N labeling, incorporation is only slightly lower with 75 and 73%, respectively, and yields are typically twofold reduced. The media were optimized for isotope incorporation, reproducibility, simplicity and cost. High isotope incorporation levels for all labeling patterns are achieved by using labeled algal amino acid extracts and exploiting well-known biochemical pathways. The final formulation consists of just five commercially available components, at costs 12-fold lower than labeling media from vendors. The approach was applied to several cytosolic and secreted target proteins.
对于众多备受关注的蛋白质而言,核磁共振(NMR)研究的主要障碍是缺乏用于同位素标记的经济实惠的真核表达系统。在此,我们提出了一种简单且经济的方案,可在用于结构生物学的最常用真核表达系统,即草地贪夜蛾昆虫细胞中生产均匀标记的蛋白质。对于¹⁵N和¹³C,掺入水平可达80%,产量与在完全培养基中表达相当。对于²H、¹⁵N和²H、¹³C、¹⁵N标记,掺入率分别仅略低,为75%和73%,产量通常降低两倍。对培养基进行了优化,以实现同位素掺入、重现性、简便性和成本的平衡。通过使用标记的藻类氨基酸提取物并利用众所周知的生化途径,可实现所有标记模式的高同位素掺入水平。最终配方仅由五种市售成分组成,成本比供应商的标记培养基低12倍。该方法已应用于几种胞质和分泌型靶蛋白。