Carter A P, Clemons W M, Brodersen D E, Morgan-Warren R J, Hartsch T, Wimberly B T, Ramakrishnan V
Medical Research Council Laboratory of Molecular Biology, Hills Road, Cambridge CB2 2QH, UK.
Science. 2001 Jan 19;291(5503):498-501. doi: 10.1126/science.1057766.
Initiation of translation at the correct position on messenger RNA is essential for accurate protein synthesis. In prokaryotes, this process requires three initiation factors: IF1, IF2, and IF3. Here we report the crystal structure of a complex of IF1 and the 30S ribosomal subunit. Binding of IF1 occludes the ribosomal A site and flips out the functionally important bases A1492 and A1493 from helix 44 of 16S RNA, burying them in pockets in IF1. The binding of IF1 causes long-range changes in the conformation of H44 and leads to movement of the domains of 30S with respect to each other. The structure explains how localized changes at the ribosomal A site lead to global alterations in the conformation of the 30S subunit.
在信使核糖核酸(mRNA)的正确位置起始翻译对于准确的蛋白质合成至关重要。在原核生物中,这个过程需要三种起始因子:IF1、IF2和IF3。我们在此报告IF1与30S核糖体亚基复合物的晶体结构。IF1的结合封闭了核糖体的A位点,并使16S RNA的44螺旋中功能重要的碱基A1492和A1493翻转出来,将它们埋入IF1的口袋中。IF1的结合导致44螺旋构象发生长程变化,并导致30S的结构域彼此相对移动。该结构解释了核糖体A位点的局部变化如何导致30S亚基构象的整体改变。