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関連する概念動画

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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関連する実験動画

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

ClpXP分解機械の特異性を高める要因である.

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
まとめ

細菌のタンパク質合成が停止すると,ssrAタグが起動し,不完全なタンパク質にペプチドタグが追加されます. SspBタンパク質は,これらのタグされたタンパク質に特異的に結合し,ClpXPプロテアゼによる分解を高めます.

科学分野:

  • バクテリアの分子生物学
  • タンパク質の分解経路について
  • 遺伝子発現の調節 遺伝子発現の調節

背景:

  • バクテリアのタンパク質合成が停止すると,ssrAタグの機構が活性化します.
  • このプロセスは,新生ポリペプチド鎖に11アミノ酸ペプチドタグを追加します.
  • ssrAタグは,不完全なタンパク質を標的にして,ClpXPプロテアゼによって分解します.

研究 の 目的:

  • リボソーム関連タンパク質SspBがssrAタグされたタンパク質の分解における役割を調査する.
  • SspBがssrAタグされた基板とClpXPプロテアゼとの相互作用に影響を与えるかどうかを判断する.
  • タンパク質の分解特異性を制御するSspBの機能を明らかにする.

主な方法:

  • ssrAタグされたタンパク質とSspBの相互作用を研究した.
  • ClpXPによってssrAタグされたタンパク質の分解に対するSspBの影響を評価した.
  • sspB遺伝子に変異があるバクテリア菌株を使用した.

主要な成果:

  • SspBは,ssrAタグされたタンパク質に特異的に結合する.
  • SspBは,ClpXPによってssrAタグされたタンパク質の認識と分解を高めます.

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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

関連する実験動画

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

  • sspBの変異は,ssrAタグされたタンパク質の分解に欠陥をもたらす.
  • 結論:

    • SspBは,ClpXPプロテアゼの特異性を高める因子として作用する.
    • SspBは,タンパク質の分解のための基板選択を制御する上で重要な役割を果たします.
    • SspB媒介経路は,切断された細菌タンパク質の効率的な除去を保証します.