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相关概念视频

Ribozymes02:47

Ribozymes

13.3K
The term ribozyme is used for RNA that can act as an enzyme. Ribozymes are mainly found in selected viruses, bacteria, plant organelles, and lower eukaryotes. Ribozymes were first discovered in 1982 when Tom Cech’s laboratory observed Group I introns acting as enzymes. This was shortly followed by the discovery of another ribozyme, Ribonulcease P, by Sid Altman’s laboratory. Both Cech and Altman received the Nobel Prize in chemistry in 1989 for their work on ribozymes.
Ribozymes can...
13.3K
Ribozymes02:47

Ribozymes

3.3K
3.3K
Ribosomal RNA Synthesis02:53

Ribosomal RNA Synthesis

14.6K
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,...
14.6K
Ribosomal RNA Synthesis02:53

Ribosomal RNA Synthesis

4.1K
4.1K
RNA Interference01:23

RNA Interference

27.8K
RNA interference (RNAi) is a process in which a small non-coding RNA molecule blocks the post-transcriptional expression of a gene by binding to its messenger RNA (mRNA) and preventing the protein from being translated.
This process occurs naturally in cells, often through the activity of genomically-encoded microRNAs. Researchers can take advantage of this mechanism by introducing synthetic RNAs to deactivate specific genes for research or therapeutic purposes. For example, RNAi could be used...
27.8K
Riboswitches01:56

Riboswitches

9.5K
Riboswitches are non-coding mRNA domains that regulate the transcription and translation of downstream genes without the help of proteins. Riboswitches bind directly to a metabolite and can form unique stem-loop or hairpin structures in response to the amount of the metabolite present. They have two distinct regions – a metabolite-binding aptamer and an expression platform.
The aptamer has high specificity for a particular metabolite which allows riboswitches to specifically regulate...
9.5K

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相关实验视频

Updated: Jan 13, 2026

DNAzyme-dependent Analysis of rRNA 2&#8217;-O-Methylation
09:12

DNAzyme-dependent Analysis of rRNA 2’-O-Methylation

Published on: September 16, 2019

8.7K

基因编码RNA滴的生长,溶解和分离,由Ribozyme催化剂.

Franziska Giessler1, William Verstraeten1, Tobias Abele1

  • 1Biophysical Engineering Group, Center for Molecular Biology of Heidelberg University (ZMBH), Heidelberg University, Heidelberg, Germany.

Angewandte Chemie (International ed. in English)
|January 7, 2026
PubMed
概括
此摘要是机器生成的。

研究人员创造了活跃的RNA滴,可以溶解和再生,由遗传信息控制. 这一突破使可编程,可进化的材料成为可能,并推进了合成细胞的建造.

关键词:
活跃滴滴剂活动滴滴剂.液态液态相隔离器 液态液态相隔离器在RNA纳米技术上.利博酶催化剂的催化作用合成细胞是一种合成细胞.

更多相关视频

Artificial RNA Polymerase II Elongation Complexes for Dissecting Co-transcriptional RNA Processing Events
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Artificial RNA Polymerase II Elongation Complexes for Dissecting Co-transcriptional RNA Processing Events

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Studying Ribonucleotide Incorporation: Strand-specific Detection of Ribonucleotides in the Yeast Genome and Measuring Ribonucleotide-induced Mutagenesis
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Studying Ribonucleotide Incorporation: Strand-specific Detection of Ribonucleotides in the Yeast Genome and Measuring Ribonucleotide-induced Mutagenesis

Published on: July 26, 2018

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相关实验视频

Last Updated: Jan 13, 2026

DNAzyme-dependent Analysis of rRNA 2&#8217;-O-Methylation
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DNAzyme-dependent Analysis of rRNA 2’-O-Methylation

Published on: September 16, 2019

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Artificial RNA Polymerase II Elongation Complexes for Dissecting Co-transcriptional RNA Processing Events
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Artificial RNA Polymerase II Elongation Complexes for Dissecting Co-transcriptional RNA Processing Events

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Studying Ribonucleotide Incorporation: Strand-specific Detection of Ribonucleotides in the Yeast Genome and Measuring Ribonucleotide-induced Mutagenesis
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Studying Ribonucleotide Incorporation: Strand-specific Detection of Ribonucleotides in the Yeast Genome and Measuring Ribonucleotide-induced Mutagenesis

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科学领域:

  • * 合成生物学 * 合成生物学
  • * 生物物理 生物物理
  • * 材料科学 材料科学

背景情况:

  • * 活跃滴,无膜,是早期生命和合成细胞的关键模型.
  • * 用遗传信息编程动态行为对于可进化的系统至关重要.

研究的目的:

  • * 用可编程序列的动态来设计暂时活跃的RNA滴.
  • * 建立合成原细胞的基因编码生命周期.
  • * 开发观察和控制随时间推移滴滴行为的方法.

主要方法:

  • *将 ribozyme 催化部位集成到 RNA 纳米恒星序列中进行自我组装.
  • *通过现场光聚合在水凝中捕获单个滴滴,用于观察.
  • *利用不同的 ribozymes (头,发针) 来控制降解动力学.
  • * 采用特定序列的RNA裂变来触发滴滴分离.
  • * 封装DNA模板用于滴滴再生.

主要成果:

  • *成功创建了顺序控制溶解的暂时活性RNA滴.
  • *使用头 (快速) 和头 (缓慢) ribozymes 证明可编程的降解速率.
  • * 通过特定序列的分离,实现混合滴滴群体的分离.
  • * 建立了一个最小的,基因编码的液滴溶解和再生循环的原理证明.
  • *直接将RNA序列与滴滴稳定性,成分和生命周期动态联系起来.

结论:

  • * 开发了一个强大的平台,用于工程可变材料.
  • * 推进了可编程生命周期的合成细胞的自下而上的构建.
  • * 证明了基因信息控制活跃滴的行为潜力.