Romby P, Wakao H, Westhof E, Grunberg-Manago M, Ehresmann B, Ehresmann C, Ebel J P
Institut de Biologie Moléculaire et Cellulaire du CNRS, Strasbourg, France.
Biochim Biophys Acta. 1990 Aug 27;1050(1-3):84-92. doi: 10.1016/0167-4781(90)90146-s.
The conformation of the E. coli initiator tRNA and of the 16S rRNA at different steps leading to the 30S.IF2.fMet-ARN(fMet).AUG.GTP complex has been investigated using several structure-specific probes. As compared to elongator tRNA, the initiator tRNA exhibits specific structural features in the anticodon arm, the T and D loops and the acceptor arm. Initiation factor 2 (IF2) interacts with the T-loop and the minor groove of the T stem of the RNA, and induces an increased flexibility in the anticodon arm. In the 30S initiation complex, additional protection is observed in the acceptor stem and in the anticodon arm of the tRNA. Within the 30S subunit, IF2 does not significantly shield defined portions of 16S rRNA, but induces both reduction and enhancement of reactivity scattered in the entire molecule. Most are constrained in a region corresponding to the cleft, the lateral protrusion and the part of the head facing the protrusion. All the reactivity changes induced by the binding of IF2 are still observed in the presence of the initiator tRNA and AUG message. The additional changes induced by the tRNA are mostly centered around the cleft-head-lateral protrusion region, near positions affected by IF2 binding.
利用多种结构特异性探针,研究了大肠杆菌起始tRNA以及在形成30S.IF2.fMet-ARN(fMet).AUG.GTP复合物的不同步骤中16S rRNA的构象。与延伸tRNA相比,起始tRNA在反密码子臂、T环和D环以及接受臂中表现出特定的结构特征。起始因子2(IF2)与RNA的T环和T茎的小沟相互作用,并诱导反密码子臂的灵活性增加。在30S起始复合物中,在tRNA的接受茎和反密码子臂中观察到额外的保护作用。在30S亚基内,IF2不会显著屏蔽16S rRNA的特定部分,但会诱导整个分子中反应性的降低和增强。大多数反应性变化集中在对应于裂隙、侧向突出部以及头部面向突出部的部分的区域。在起始tRNA和AUG信息存在的情况下,仍然可以观察到由IF2结合诱导的所有反应性变化。tRNA诱导的额外变化大多集中在裂隙-头部-侧向突出部区域,靠近受IF2结合影响的位置。