Risuleo G, Gualerzi C, Pon C
Eur J Biochem. 1976 Aug 16;67(2):603-13. doi: 10.1111/j.1432-1033.1976.tb10726.x.
Initiation factor IF-3 causes the destabilization of preformed ternary complexes of 30-S ribosomal subunit, codons and aminoacyl-tRNAs or peptidyl-tRNA. This destabilization is dilution-dependent and affects all ternary complexes with the exception of those containing the initiator fMet-tRNA, which remain more resistant to IF-3-induced destabilization under the various conditions studied. Several possible reasons for this specificity have been examined. It was found that the basis for the specificity is not: (a) an intrinsic greater stability of the ternary complexes containing fMet-tRNA, (b) the amoung of aminoacyl-tRNA bound to the ribosome, (c) the conditions under which the ternary complex is made or (d) the formylation of the amino group. On the other hand, the nature of the polynucleotide in response to which the ternary complex is formed was found to influence the amount of aminoacyl-tRan bound to the ribosome, and to some extent the amount of aminoacyl-tRNA which can be relased. The ternary complex containing the mischarged initiator tRNA fVal-tRNAfMet displays greater resistance to the IF-3-induced destabilization than the complex containing fVal-tRNAVal. These results indicate that the specificity of the IF-3 activity is due to the special structural feature of the initiator tRNA molecule and to some extent to the nature of the polynucleotide. The IF-3-induced destabilization of ternary complexes was found to be little affected by variations in reaction conditons, so that this IF-3 activity can be used to measure the stoichiometric binding of IF-3 to the ribosome over a broad range of pH and K+ and Mg2+ concentrations. Several antibiotics have been tested for their capacity to interfere with this reaction; only high concentrations of tetracycline blocked this IF-3 activity.
起始因子IF-3会导致预先形成的30-S核糖体亚基、密码子与氨酰-tRNA或肽基-tRNA三元复合物的不稳定。这种不稳定依赖于稀释作用,并且会影响所有的三元复合物,但含有起始甲硫氨酰-tRNA的复合物除外,在各种研究条件下,这些复合物对IF-3诱导的不稳定更具抗性。已经研究了造成这种特异性的几个可能原因。结果发现,特异性的基础不是:(a) 含有甲硫氨酰-tRNA的三元复合物本身具有更高的稳定性;(b) 与核糖体结合的氨酰-tRNA的量;(c) 形成三元复合物的条件;(d) 氨基的甲酰化。另一方面,发现形成三元复合物所响应的多核苷酸的性质会影响与核糖体结合的氨酰-tRNA的量,并且在一定程度上会影响可释放的氨酰-tRNA的量。含有错配起始tRNA fVal-tRNAfMet的三元复合物比含有fVal-tRNAVal的复合物对IF-3诱导的不稳定具有更高的抗性。这些结果表明,IF-3活性的特异性归因于起始tRNA分子的特殊结构特征,并且在一定程度上归因于多核苷酸的性质。发现反应条件的变化对IF-3诱导的三元复合物不稳定影响很小,因此这种IF-3活性可用于在广泛的pH、K+和Mg2+浓度范围内测量IF-3与核糖体的化学计量结合。已经测试了几种抗生素干扰该反应的能力;只有高浓度的四环素会阻断这种IF-3活性。