Dabrowski M, Spahn C M, Nierhaus K H
Max-Planck-Institut für Molekulare Genetik, AG Ribosomen, Berlin, Germany.
EMBO J. 1995 Oct 2;14(19):4872-82. doi: 10.1002/j.1460-2075.1995.tb00168.x.
In vitro transcribed tRNA(Phe) analogues from Escherichia coli containing up to four randomly distributed A, G, U or C phosphorothioated nucleotides were used to investigate contact patterns with the ribosome in the A and P sites. The tRNAs were biologically active. Molecular iodine (I2) can trigger a break in the sugar-phosphate backbone at phosphorothioated positions of the ribosomal bound tRNAs if contacts with ribosomal components do not prevent access of the iodine. Highly differentiated protection patterns were found which were strikingly different in the A and P sites, respectively. Strong protections accumulated in the T psi C loop and no protection was seen in the extra-arm region in both sites, whereas the phosphates in the anticodon loop are more strongly protected in the A site. Strong common protections in both the A and P sites were found neighbouring universally or semi-universally conserved bases in prominent regions of the tertiary structure of tRNAs: Y11, Y32, U33, psi55, C56, A58 and Y60. These bases are therefore candidates for 'identity elements' in ribosomal tRNA recognition. The data further indicate that tRNAs change their conformations upon binding to either ribosomal site.
使用来自大肠杆菌的体外转录的tRNA(Phe)类似物,其含有多达四个随机分布的A、G、U或C硫代磷酸化核苷酸,来研究与核糖体A和P位点的接触模式。这些tRNA具有生物活性。如果与核糖体组分的接触不阻止碘的进入,分子碘(I2)可以在核糖体结合的tRNA的硫代磷酸化位置引发糖-磷酸主链的断裂。发现了高度分化的保护模式,它们在A和P位点分别显著不同。在TψC环中积累了强烈的保护,在两个位点的额外臂区域均未观察到保护,而反密码子环中的磷酸在A位点受到更强的保护。在tRNA三级结构突出区域中与普遍或半普遍保守碱基相邻的位置,在A和P位点均发现了强烈的共同保护:Y11、Y32、U33、ψ55、C56、A58和Y60。因此,这些碱基是核糖体tRNA识别中“识别元件”的候选者。数据进一步表明,tRNA在与任一核糖体位点结合时会改变其构象。