Geigenmüller U, Nierhaus K H
Eur J Biochem. 1986 Dec 15;161(3):723-6. doi: 10.1111/j.1432-1033.1986.tb10499.x.
A and P sites of Escherichia coli ribosomes were titrated with AcPhe-tRNAPhe, in the absence or presence of tetracycline. The P-site location of the bound AcPhe-tRNA was assessed by means of a quantitative puromycin reaction. The results demonstrate that, in agreement with the generally held view, tetracycline exclusively inhibits the A-site binding, if the statistical number of bound acyl-tRNA molecules per ribosome does not exceed about 0.5. However, above this value the P site becomes sensitive to tetracycline as well. It follows that the tightly coupled 70S ribosomes used in functional studies appear to be functionally heterogeneous, i.e. those P sites which cannot be affected by tetracycline are preferentially occupied by AcPhe-tRNA, whereas higher concentrations of this tRNA species are required to fill tetracycline-sensitive P sites. Furthermore, the results imply that under tRNA saturation conditions the tetracycline inhibition cannot be used as an indicator for the site location of bound tRNA.
在不存在或存在四环素的情况下,用乙酰苯丙氨酰 - 苯丙氨酸转运核糖核酸(AcPhe - tRNAPhe)对大肠杆菌核糖体的A位点和P位点进行滴定。通过定量嘌呤霉素反应评估结合的AcPhe - tRNA在P位点的位置。结果表明,与普遍观点一致,如果每个核糖体结合的酰基 - tRNA分子的统计数量不超过约0.5,四环素仅抑制A位点结合。然而,超过这个值时,P位点也会对四环素敏感。由此可见,功能研究中使用的紧密偶联的70S核糖体在功能上似乎是异质的,即那些不受四环素影响的P位点优先被AcPhe - tRNA占据,而填充对四环素敏感的P位点则需要更高浓度的这种转运核糖核酸。此外,结果表明在转运核糖核酸饱和条件下,四环素抑制不能用作结合的转运核糖核酸位点定位的指标。