Jones C R, Kearns D R
Proc Natl Acad Sci U S A. 1974 Oct;71(10):4237-40. doi: 10.1073/pnas.71.10.4237.
The binding of paramagnetic rare earth ions to yeast tRNA(Phe) shifts some resonances in the low-field nuclear magnetic resonance spectrum that have been assigned to ring nitrogen protons of specific Watson-Crick base pairs. The changes in the nuclear magnetic resonance spectrum as the tRNA is titrated with Eu(3+) indicate that 4 (or 5) Eu(3+) ions are tightly bound, that the metal binding is in the fast exchange limit, and that the binding to different sites in the molecule is sequential rather than cooperative. The first metal bound simultaneously shifts resonances associated with the dihydrouridine and the -C-C-A stem. This permits us to conclude that the folding of the tRNA(Phe) in solution brings the phosphate backbone of the -C-C-A and the dihydrouridine stems into close proximity. A model of the three-dimensional structure of tRNA(Phe) incorporating this new information appears to be compatible with the results obtained from x-ray diffraction.
顺磁性稀土离子与酵母苯丙氨酸转运核糖核酸(tRNA(Phe))的结合会使低场核磁共振谱中的一些共振发生位移,这些共振已被指定为特定沃森-克里克碱基对的环氮质子的共振。随着用铕(Eu(3+))对tRNA进行滴定,核磁共振谱的变化表明有4(或5)个Eu(3+)离子紧密结合,金属结合处于快速交换极限,并且与分子中不同位点的结合是顺序性的而非协同性的。第一个结合的金属同时使与二氢尿嘧啶和-C-C-A茎相关的共振发生位移。这使我们能够得出结论,溶液中tRNA(Phe)的折叠使-C-C-A和二氢尿嘧啶茎的磷酸主链紧密靠近。纳入这一新信息的tRNA(Phe)三维结构模型似乎与从X射线衍射获得的结果相符。