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Ribosomal RNA Synthesis02:53

Ribosomal RNA Synthesis

13.2K
Ribosome synthesis is a highly complex and coordinated process involving more than 200 assembly factors. The synthesis and processing of ribosomal components occurs not only in the nucleolus but also in the nucleoplasm and the cytoplasm of eukaryotic cells.
Ribosome biogenesis begins with the synthesis of 5S and 45S pre-rRNAs by distinct RNA polymerases. The primary transcripts are extensively processed and modified before they are bound and folded by ribosomal proteins and assembly factors,...
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Ribosomes01:27

Ribosomes

7.5K
Ribosomes translate genetic information encoded by messenger RNA (mRNA) into proteins. Both prokaryotic and eukaryotic cells have ribosomes. Cells that synthesize large quantities of protein—such as secretory cells in the human pancreas—can contain millions of ribosomes.
Ribosome Structure and Assembly
Ribosomes are composed of ribosomal RNA (rRNA) and proteins. In eukaryotes, rRNA is transcribed from genes in the nucleolus—a part of the nucleus that specializes in ribosome...
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Initiation of Translation02:33

Initiation of Translation

32.6K
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...
32.6K
Improving Translational Accuracy02:07

Improving Translational Accuracy

10.1K
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...
10.1K
Protein Complex Assembly02:41

Protein Complex Assembly

10.6K
Proteins can form homomeric complexes with another unit of the same protein or heteromeric complexes with different types.  Most protein complexes self-assemble spontaneously via ordered pathways, while some proteins need assembly factors that guide their proper assembly. Despite the crowded intracellular environment, proteins usually interact with their correct partners and form functional complexes.
Many viruses self-assemble into a fully functional unit using the infected host cell to...
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Directing Proteins to the Rough Endoplasmic Reticulum01:34

Directing Proteins to the Rough Endoplasmic Reticulum

7.2K
The organelle-specific signaling sequences direct proteins synthesized in the cytosol to their final destination like ER, mitochondria, peroxisomes, etc. Some of the proteins directed to ER are then trafficked via vesicles to other organelles within the cell or the extracellular environment through the Golgi complex. For example, the rough ER synthesizes soluble proteins for transportation to the lysosomes or secretion out of the cell. It can also synthesize transmembrane proteins that can...
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相关实验视频

Updated: Jun 25, 2025

Eukaryotic Polyribosome Profile Analysis
09:16

Eukaryotic Polyribosome Profile Analysis

Published on: June 15, 2010

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细胞核核糖体核糖体组装组合

Arnaud Vanden Broeck1, Sebastian Klinge1

  • 1Laboratory of Protein and Nucleic Acid Chemistry, The Rockefeller University, New York, New York, USA;

Annual review of biochemistry
|May 20, 2024
PubMed
概括
此摘要是机器生成的。

低温电子显微镜的近期进展揭示了真核核糖核糖体组装的复杂机制. 本综述详细介绍了酵母和人类核糖体子单元的形成,重点介绍了RNA折叠和校对过程.

关键词:
在RNA折叠过程中.电子显微镜的冷电子显微镜欧核细胞核糖体的核糖体是什么在rRNA处理过程中.核糖体组合组合的组合组合.核糖体生物发生的生物.

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Peering at Brain Polysomes with Atomic Force Microscopy
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相关实验视频

Last Updated: Jun 25, 2025

Eukaryotic Polyribosome Profile Analysis
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Eukaryotic Polyribosome Profile Analysis

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Examining Proteasome Assembly with Recombinant Archaeal Proteasomes and Nondenaturing PAGE: The Case for a Combined Approach
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Peering at Brain Polysomes with Atomic Force Microscopy
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科学领域:

  • 分子生物学分子生物学
  • 结构生物学 结构生物学
  • 细胞生物学 细胞生物学

背景情况:

  • 核细胞核糖体生物发生是一个复杂的过程,涉及许多组装因素.
  • 电子显微镜 (cryo-EM) 彻底改变了对核糖体组装中间体的研究.
  • 了解核糖体组合对于细胞功能和疾病研究至关重要.

研究的目的:

  • 审查目前对真核核糖核糖体组装机制的理解.
  • 要突出最近的结构和生化发现在核糖体生物发生.
  • 讨论关键概念,如RNA折叠,组装时间表和校对.

主要方法:

  • 电子显微镜 (cryo-EM) 用于结构的确定.
  • 生物化学试验用于研究因子功能和相互作用.
  • 基因方法用于识别和表征组装因子.
  • 生物信息学和计算建模.

主要成果:

  • 已经确定了许多核糖体组装中间体的详细结构.
  • 阐明了特定组装因子在指导RNA折叠和子单元关联中的关键作用.
  • 确定了强制组装时间表和酶介导过渡的机制.
  • 校对机制的证据,以确保核糖体组合的忠实性.

结论:

  • 细胞核糖体组装是一个高度规范的,逐步的过程.
  • 结构和生化数据提供了对核糖体生物发生的动态视图.
  • 进一步的研究将继续完善我们对这种基本细胞过程的理解.