一个真核转化启动复合体的分子架构
Israel S Fernández1, Xiao-Chen Bai1, Tanweer Hussain1
1MRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge Biomedical Campus, CB2 0QH, United Kingdom.
概括
研究人员使用冷电子显微镜可视化了真核生物的转化启动复合体. 这项研究揭示了启动因子eIF5B的关键构造变化,这对蛋白质合成至关重要.
科学领域:
- 分子生物学分子生物学
- 结构生物学 结构生物学
- 生物化学 生物化学
背景情况:
- 细胞转化启动是一个复杂的过程,涉及核糖体子单元的连接.
- 启动因子eIF5B催化最后一步,确保正确的mRNA和启动tRNA定位.
- 了解这一步骤对于理解蛋白质合成调节至关重要.
研究的目的:
- 为了确定eIF5B启动复合体的高分辨率结构.
- 为了阐明eIF5B,tRNA和核糖体在启动过程中的构造变化.
- 探索eIF5B促进翻译启动的机制.
主要方法:
- 使用冷电子显微镜 (cryo-EM) 来分析eIF5B启动复合体.
- 处理了一小部分 (<3%) 不同质的样本粒子 (5143个粒子).
- 为复杂的结构实现了6.6安格斯特罗姆的分辨率.
主要成果:
- 在6.6安格斯特罗姆分辨率下确定了eIF5B启动复合物的结构.
- 在eIF5B,启动器tRNA (Met-tRNAiMet) 和核糖体中观察到显著的构造变化.
- 该结构为eIF5B在核糖体子单元连接中的功能提供了详细的见解.
结论:
- 从一个小而异质的样本获得的高分辨率表明了研究动态复杂的新方法.
- 结构洞察力澄清了eIF5B在促进真核细胞转化启动中的机制.
- 该方法可用于描述其他过渡性或动态生物复合物的特征.
相关概念视频
Initiation of Translation
24.8K
Initiating translation is complex because it involves multiple molecules. Initiator tRNA, ribosomal subunits, and eukaryotic initiation factors (eIFs) are all required to assemble on the initiation codon of mRNA. This process consists of several steps that are mediated by different eIFs.
First, the initiator tRNA must be selected from the pool of elongator tRNAs by eukaryotic initiation factor 2 (eIF2). The initiator tRNA (Met-tRNAi) has conserved sequence elements including modified bases at...
First, the initiator tRNA must be selected from the pool of elongator tRNAs by eukaryotic initiation factor 2 (eIF2). The initiator tRNA (Met-tRNAi) has conserved sequence elements including modified bases at...
24.8K
Initiation of Translation
7.0K
7.0K
Translation in Prokaryotes
2.9K
Prokaryote translation is a complex, highly coordinated process that converts genetic information from mRNA into functional proteins. It involves three stages: initiation, elongation, and termination, each facilitated by specific molecular components.Initiation of TranslationThe process begins with the assembly of the ribosomal subunits and initiation factors on the mRNA. In bacteria, the 30S ribosomal subunit recognizes the Shine-Dalgarno sequence in the mRNA, a conserved region upstream of...
2.9K
Improving Translational Accuracy
11.6K
Base complementarity between the three base pairs of mRNA codon and the tRNA anticodon is not a failsafe mechanism. Inaccuracies can range from a single mismatch to no correct base pairing at all. The free energy difference between the correct and nearly correct base pairs can be as small as 3 kcal/ mol. With complementarity being the only proofreading step, the estimated error frequency would be one wrong amino acid in every 100 amino acids incorporated. However, error frequencies observed in...
11.6K
Termination of Translation
19.7K
The large ribosomal subunit has several important structures essential to translation. These include the peptidyl transferase center (PTC) - which is the site where the peptide bond is formed - and a large, internal, water-filled tube through which the nascent polypeptide moves. This latter structure is called the Peptide Exit Tunnel, and it begins at the PTC and spans the body of the large ribosomal subunit. During translation, as the nascent polypeptide chain is synthesized, it passes through...
19.7K
Cotranslational Protein Translocation
8.4K
Translocation of proteins across membranes is an ancient process that occurs even in bacteria and archaebacteria. In fact, the components of the translocation machinery are still conserved between prokaryotes and eukaryotes.
Sec61 channel partners for cotranslational translocation
During cotranslational translocation, the Sec61 channel partners with the signal recognition particle (SRP), the signal recognition particle receptor (SR), and the ribosomes to transport the nascent polypeptide chain...
Sec61 channel partners for cotranslational translocation
During cotranslational translocation, the Sec61 channel partners with the signal recognition particle (SRP), the signal recognition particle receptor (SR), and the ribosomes to transport the nascent polypeptide chain...
8.4K


