Tate W P, Hornig H, Lührmann R
J Biol Chem. 1983 Sep 10;258(17):10360-5.
Recognition of the termination codon by release factor was studied with 70 S ribosomes containing initiator tRNA at the P site and an amino acid-specifying codon as well as the corresponding cognate tRNA at the A site. In vitro termination was not excluded when either the A site was occupied with an amino acid-specifying codon or the termination codon was displaced from the A site codon position by spacer nucleotides between UAA and the P site bound AUG. The release factor may have flexibility in its codon recognizing domain to be able to adjust to this enforced change in the position of the termination codon on the ribosome without loss of functional specificity. Deacylated tRNA bound at the A site of 70 S ribosomes did not interfere with stoichiometric UAA-directed release factor binding to these particles. In contrast, a ternary complex (aminoacyl-tRNA elongation factor-Tu . GTP) abolished the binding of the release factor while aminoacyl-tRNA inhibited it only weakly. This suggests that release factor and elongation factor-Tu have overlapping binding sites but the A site binding domains of the release factor and tRNA are exclusive.
利用在P位点含有起始tRNA、在A位点含有氨基酸特异性密码子以及相应同源tRNA的70S核糖体,研究了释放因子对终止密码子的识别。当A位点被氨基酸特异性密码子占据,或者终止密码子通过UAA与P位点结合的AUG之间的间隔核苷酸从A位点密码子位置移位时,体外终止并未被排除。释放因子在其密码子识别结构域可能具有灵活性,以便能够适应核糖体上终止密码子位置的这种强制变化而不丧失功能特异性。结合在70S核糖体A位点的脱酰基tRNA不会干扰化学计量的UAA指导的释放因子与这些颗粒的结合。相反,三元复合物(氨酰-tRNA延伸因子-Tu·GTP)消除了释放因子的结合,而氨酰-tRNA仅微弱地抑制它。这表明释放因子和延伸因子-Tu具有重叠的结合位点,但释放因子和tRNA的A位点结合结构域是相互排斥的。