Iwai Hideo, Fiaux Jocelyne
Research Program in Structural Biology and Biophysics, Institute of Biotechnology, University of Helsinki, P.O. Box 65, Helsinki, 00014, Finland.
J Biomol NMR. 2007 Mar;37(3):187-93. doi: 10.1007/s10858-006-9124-8. Epub 2007 Jan 13.
We describe a simple approach to classify amino acid residue types in NMR spectra of proteins for supporting the backbone resonance assignments. It makes use of the differences in biosynthetic pathways of the 20 amino acids in Escherichia coli. Therefore, it is distinct from the parameters routinely exploited in the backbone resonance assignment such as chemical shifts and spin topology information. The combination of biosynthetically directed fractional 13C-labeling and uniform 15N-labeling enables us to obtain both residue-type specific information and sequential connectivities from a single protein sample. The residue-type classification exploiting biosynthetic pathways can be used for accelerating the conventional backbone assignment procedure.
我们描述了一种简单的方法,用于在蛋白质的核磁共振光谱中对氨基酸残基类型进行分类,以辅助主链共振归属。该方法利用了大肠杆菌中20种氨基酸生物合成途径的差异。因此,它与主链共振归属中常规使用的参数不同,如化学位移和自旋拓扑信息。生物合成导向的分数13C标记与均匀15N标记相结合,使我们能够从单个蛋白质样品中获得残基类型特异性信息和序列连接性。利用生物合成途径进行的残基类型分类可用于加速传统的主链归属过程。