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用于核磁共振分析的大肠杆菌转运RNA的15N和13C标记

15N and 13C labeling of Escherichia coli tRNAs toward the NMR analysis.

作者信息

Kawai G, Takayanagi M, Hayashi N, Niimi T, Sanpei G, Mizobuchi K, Miyazawa T, Tokoyama S, Watanabe K

机构信息

Faculty of Engineering, University of Tokyo, Japan.

出版信息

Nucleic Acids Symp Ser. 1992(27):131-2.

PMID:1283902
Abstract

Escherichia coli tRNAs were labeled with stable isotope 15N in vivo. Three species of tRNA, tRNA(Glu), tRNA(Lys) and tRNA(Ile), were purified by an HPLC system and their NMR spectra were observed. In heteronuclear 1H-15N multiple or single quantum coherence (HMQC or HSQC) spectra, the crosspeaks corresponding to NH3 of U and NH1 of G can be distinguished clearly since their 15N chemical shifts are significantly different from each other. Thus, this combination of 15N-labeling and the proton detected heteronuclear experiments are useful for the signal assignment and the conformational analysis of tRNAs. Furthermore, C1'- selective 13C-labeling of nucleotides was examined in vivo in order to resolve the H1' signals of tRNAs. By using a newly constructed E. coli mutant strain, the isotopic enrichments of more than 90% at C1' and of less than 10% for other ribose carbons were achieved.

摘要

大肠杆菌的转运RNA(tRNA)在体内用稳定同位素15N进行标记。通过高效液相色谱(HPLC)系统纯化了三种tRNA,即tRNA(Glu)、tRNA(Lys)和tRNA(Ile),并观察了它们的核磁共振(NMR)光谱。在异核1H-15N多量子或单量子相干(HMQC或HSQC)光谱中,由于U的NH3和G的NH1的15N化学位移彼此显著不同,因此可以清楚地区分对应于它们的交叉峰。因此,15N标记与质子检测异核实验的这种组合对于tRNA的信号归属和构象分析是有用的。此外,为了解析tRNA的H1'信号,在体内对核苷酸的C1'-选择性13C标记进行了研究。通过使用新构建的大肠杆菌突变菌株,实现了C1'处超过90%的同位素富集以及其他核糖碳处低于10%的同位素富集。

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