Adwaith B Uday, Rishi Kumar Mishra, Tanweer Hussain
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引用次数: 0
摘要
在翻译的初始步骤中,细菌核糖体需要三个启动因子 IF1、IF2 和 IF3。这些 IF 可确保启动子 tRNA 反密码子与位于 30S 核糖体亚基 P 位点的 mRNA 中的起始密码子正确碱基配对。IF3 是最先与 30S 结合的 IF 之一,在选择正确的起始密码子和密码子:反密码子碱基配对中起着至关重要的作用。IF3 还能防止核糖体 50S 亚基过早结合,帮助核糖体循环。据报道,IF3 会改变结合位点和构象,以确保翻译启动的保真度。最近的一项研究表明,IF3 CTD 的初始结合点远离 P 位点,而 IF1 和 IF2 会促进 CTD 向 P 位点移动,同时促进 NTD 移动。因此,为了在没有其他 IF 的情况下观察 IF3 的位置,我们测定了 30S-IF3 复合物的冷冻电镜结构。该结构图显示,即使在没有 IF1 和 IF2 的情况下,IF3 也以扩展构象存在,CTD 位于 P 位点,NTD 位于平台附近。因此,IF3 CTD 与 P 位点结合,并在翻译启动后期将启动子 tRNA 容纳在 P 位点时移开。总之,我们报告的 30S-IF3 结构揭示了 IF3 在 30S 核糖体亚基上的起始结合位点和构象。
Initiation factor 3 bound to the 30S ribosomal subunit in an initial step of translation.
Bacterial ribosomes require three initiation factors IF1, IF2, and IF3 during the initial steps of translation. These IFs ensure correct base pairing of the initiator tRNA anticodon with the start codon in the mRNA located at the P-site of the 30S ribosomal subunit. IF3 is one of the first IFs to bind to the 30S and plays a crucial role in the selection of the correct start codon and codon: anticodon base pairing. IF3 also prevents the premature association of the 50S subunit of ribosomes and aids in ribosome recycling. IF3 is reported to change binding sites and conformation to ensure translation initiation fidelity. A recent study suggested an initial binding of IF3 CTD away from the P-site and that IF1 and IF2 promote the movement of CTD to the P-site and concomitant movement of NTD. Hence, to visualize the position of IF3 in the absence of any other IFs, we determined cryo-EM structure of the 30S-IF3 complex. The map shows that IF3 is present in an extended conformation with CTD present at the P-site and NTD near the platform even in the absence of IF1 and IF2. Hence, IF3 CTD binds at the P-site and moves away during the accommodation of the initiator tRNA at the P-site in the later steps of translation initiation. Overall, we report the structure of 30S-IF3 which demystifies the starting binding site and conformation of IF3 on the 30S ribosomal subunit.
期刊介绍:
PROTEINS : Structure, Function, and Bioinformatics publishes original reports of significant experimental and analytic research in all areas of protein research: structure, function, computation, genetics, and design. The journal encourages reports that present new experimental or computational approaches for interpreting and understanding data from biophysical chemistry, structural studies of proteins and macromolecular assemblies, alterations of protein structure and function engineered through techniques of molecular biology and genetics, functional analyses under physiologic conditions, as well as the interactions of proteins with receptors, nucleic acids, or other specific ligands or substrates. Research in protein and peptide biochemistry directed toward synthesizing or characterizing molecules that simulate aspects of the activity of proteins, or that act as inhibitors of protein function, is also within the scope of PROTEINS. In addition to full-length reports, short communications (usually not more than 4 printed pages) and prediction reports are welcome. Reviews are typically by invitation; authors are encouraged to submit proposed topics for consideration.