Choi B S, Redfield A G
Graduate Department of Biochemistry, Brandeis University, Waltham, Massachusetts 02254.
Biochemistry. 1992 Dec 29;31(51):12799-802. doi: 10.1021/bi00166a013.
1,3-15N-Labeled uracil was synthesized chemically and used to prepare labeled Escherichia coli tRNA(Val) biosynthetically. 500-MHz measurements of 15N and proton chemical shift were obtained, for all uridine and uridine-related bases, by heteronuclear multiple-quantum coherence spectroscopy. All the uracil NH group resonances were assigned and were in agreement with previous proton-only assignments. The temperature dependence of intensities of resonances was used to infer the relative stability of parts of the molecule. The acceptor stem was the least thermally stable structural feature, while the anticodon and T loop were relatively more stable.
化学合成了1,3 - 15N标记的尿嘧啶,并用于生物合成制备标记的大肠杆菌tRNA(Val)。通过异核多量子相干光谱法获得了所有尿苷和与尿苷相关碱基的15N和质子化学位移的500兆赫兹测量值。所有尿嘧啶NH基团共振均已确定,且与先前仅基于质子的确定结果一致。利用共振强度的温度依赖性来推断分子各部分的相对稳定性。受体茎是热稳定性最低的结构特征,而反密码子和T环相对更稳定。