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相关概念视频

The Replisome03:01

The Replisome

DNA replication is carried out by a large complex of proteins that act in a coordinated matter to achieve high-fidelity DNA replication. Together this complex is known as the DNA replication machinery or the replisome.
The synthesis of the leading and lagging strands is a highly coordinated process. To explain this, the “Trombone model” was proposed by Bruce Alberts in 1980. The DNA loop formation starts when a primer is synthesized on the parent lagging strand. The loop grows with the...
Conservative Site-specific Recombination and Phase Variation02:53

Conservative Site-specific Recombination and Phase Variation

Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...
Coordination of Gene Expression Processes in Bacteria01:29

Coordination of Gene Expression Processes in Bacteria

The DNA replication, transcription, and translation processes are intricately coupled in bacteria, allowing efficient gene expression and rapid protein synthesis. While this physical and functional coordination is advantageous, it introduces challenges that bacteria overcome through specific regulatory mechanisms.Coupling of Replication, Transcription, and TranslationThe coupling of replication, transcription, and translation is a hallmark of bacterial gene expression. As the replisome unwinds...

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相关实验视频

Updated: Jul 12, 2026

Membrane-SPINE: A Biochemical Tool to Identify Protein-protein Interactions of Membrane Proteins In Vivo
10:53

Membrane-SPINE: A Biochemical Tool to Identify Protein-protein Interactions of Membrane Proteins In Vivo

Published on: November 7, 2013

对于ClpXP降解机的特异性增强因素.

I Levchenko1, M Seidel, R T Sauer

  • 1Department of Biology and Howard Hughes Medical Institute, Building 68, Room 523, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA 02139, USA.

Science (New York, N.Y.)
|September 29, 2000
PubMed
概括

细菌蛋白质合成停止触发ssrA标记,将标签添加到不完整的蛋白质中. 该SspB蛋白特别结合这些标记蛋白质,增强其由ClpXP蛋白酶降解.

科学领域:

  • 细菌分子生物学 细菌分子生物学
  • 蛋白质降解途径 蛋白质降解途径
  • 基因表达调节 基因表达调节

背景情况:

  • 停滞的细菌蛋白质合成激活了ssrA标记机制.
  • 这一过程将11个氨基酸标签添加到新生的多链中.
  • 该ssrA标签针对不完整的蛋白质,以降解ClpXP蛋白酶.

研究的目的:

  • 调查核糖体相关蛋白SspB在ssrA标记蛋白质降解中的作用.
  • 为了确定SspB是否影响ssrA标记基质和ClpXP蛋白酶之间的相互作用.
  • 阐明SspB在控制蛋白质降解特异性的功能.

主要方法:

  • 研究了SspB与ssrA标记蛋白的相互作用.
  • 评估了SspB对ClpXP对ssrA标记蛋白质的降解的影响.
  • 使用了具有sspB基因突变的细菌菌株.

主要成果:

  • SspB 特别与 ssrA 标记的蛋白质结合.
  • SspB增强了ClpXP对ssrA标记蛋白的识别和降解.
  • 在sspB中的突变导致ssrA标记蛋白质降解的缺陷.

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Engineering Artificial Factors to Specifically Manipulate Alternative Splicing in Human Cells
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Identifying Amino Acid Overproducers Using Rare-Codon-Rich Markers

Published on: June 24, 2019

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Last Updated: Jul 12, 2026

Membrane-SPINE: A Biochemical Tool to Identify Protein-protein Interactions of Membrane Proteins In Vivo
10:53

Membrane-SPINE: A Biochemical Tool to Identify Protein-protein Interactions of Membrane Proteins In Vivo

Published on: November 7, 2013

Engineering Artificial Factors to Specifically Manipulate Alternative Splicing in Human Cells
10:06

Engineering Artificial Factors to Specifically Manipulate Alternative Splicing in Human Cells

Published on: April 26, 2017

Identifying Amino Acid Overproducers Using Rare-Codon-Rich Markers
10:41

Identifying Amino Acid Overproducers Using Rare-Codon-Rich Markers

Published on: June 24, 2019

结论:

  • SspB 作为 ClpXP 蛋白酶的特异性增强因子.
  • 在控制蛋白质降解的基质选择方面,SspB起着至关重要的作用.
  • 由SspB介导的途径确保有效地去除截断的细菌蛋白质.