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関連する概念動画

Homologous Recombination02:31

Homologous Recombination

The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...
ER Retrieval Pathway01:45

ER Retrieval Pathway

In the secretory pathway, vesicles transport proteins from one cellular compartment to another in forward transport to deliver the protein to its correct location. Occasionally, misfolded proteins and incorrect proteins escape their original compartments, and a retrieval pathway is used to return the escaped proteins to their original compartment.
The ER uses many checkpoints to prevent the entry of incorrectly folded or a resident protein as cargo onto a transport vesicle. These mechanisms...
The Unfolded Protein Response01:37

The Unfolded Protein Response

The ER is the hub of protein synthesis in a cell. It has robust systems to quality control protein folding and also for degradation of terminally misfolded proteins. Under normal conditions, a small proportion of misfolded proteins that cannot be salvaged need to be transported to the cytoplasm by the ER-associated degradation or ERAD pathways. However, if the ERAD cannot handle the misfolded proteins, the cell activates the unfolded protein response or UPR to adjust the protein folding...
Export of Misfolded Proteins out of the ER01:32

Export of Misfolded Proteins out of the ER

After folding, the ER assesses the quality of secretory and membrane proteins. The correctly folded proteins are cleared by the calnexin cycle for transport to their final destination, while misfolded proteins are held back in the ER lumen. The ER chaperones attempt to unfold and refold the misfolded proteins but sometimes fail to achieve the correct native conformation. Such terminally misfolded proteins are then exported to the cytosol by ER-associated degradation or ERAD pathway for...
Hazard Ratio01:12

Hazard Ratio

The hazard ratio (HR) is a widely used measure in clinical trials to compare the risk of events, such as death or disease recurrence, between two groups over time. It reflects the ratio of hazard rates—the instantaneous risk of the event occurring—between a treatment group and a control group. This measure provides valuable insights into the relative effectiveness of a treatment by assessing how the risk of an event differs between the two groups.
For example, in a clinical trial evaluating a...

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関連する実験動画

Updated: May 11, 2026

Growth-based Determination and Biochemical Confirmation of Genetic Requirements for Protein Degradation in Saccharomyces cerevisiae
10:57

Growth-based Determination and Biochemical Confirmation of Genetic Requirements for Protein Degradation in Saccharomyces cerevisiae

Published on: February 16, 2015

人事部ってあるの? ERADの理解は可能だ!

Nurzian Ismail1, Davis T W Ng

  • 1Temasek Life Sciences Laboratory and Department of Biological Sciences, National University of Singapore, Singapore 117604.

Cell
|July 29, 2006
PubMed
まとめ

エンドプラズマの網膜膜にある2つのタンパク質複合体は,特定の誤折りたたまれたタンパク質を認識し,分解する. この発見は,重要な細胞プロセスであるタンパク質の品質管理における基板特異性を明らかにします.

科学分野:

  • 細胞生物学 細胞生物学
  • タンパク質の分解 タンパク質の分解
  • エンドプラズマ網膜の機能

背景:

  • 誤った折り畳まれたタンパク質は,細胞の健康に脅威をもたらす.
  • 特定のタンパク質の分解のメカニズムは完全に理解されていません.
  • エンドプラズマ網膜は,タンパク質の折りたたみと品質管理の重要な場所です.

研究 の 目的:

  • タンパク質の分解における基板特異性のメカニズムを解明する.
  • 間違った折りたたまれたタンパク質を認識し,分解するタンパク質因子を特定する.
  • タンパク質品質管理におけるエンドプラズマ網膜の役割を理解する.

主な方法:

  • エンドプラズマの網膜膜にあるタンパク質複合体を研究した.
  • タンパク質の基質を特定するために生化学的および遺伝的アプローチを使用しました.
  • 特定のタンパク質サブセットの認識と分解経路を分析した.

主要な成果:

  • エンドプラズマ網膜膜で2つの異なるタンパク質複合体を特定しました.
  • これらの複合体は,間違った折りたたまれたタンパク質の特定のサブセットを認識する責任を負うことが示されました.

さらに関連する動画

Genetic Variant Detection in the CALR gene using High Resolution Melting Analysis
08:46

Genetic Variant Detection in the CALR gene using High Resolution Melting Analysis

Published on: August 26, 2020

RBDT: A Computerized Task System based in Transposition for the Continuous Analysis of Relational Behavior Dynamics in Humans
11:09

RBDT: A Computerized Task System based in Transposition for the Continuous Analysis of Relational Behavior Dynamics in Humans

Published on: July 17, 2021

関連する実験動画

Last Updated: May 11, 2026

Growth-based Determination and Biochemical Confirmation of Genetic Requirements for Protein Degradation in Saccharomyces cerevisiae
10:57

Growth-based Determination and Biochemical Confirmation of Genetic Requirements for Protein Degradation in Saccharomyces cerevisiae

Published on: February 16, 2015

Genetic Variant Detection in the CALR gene using High Resolution Melting Analysis
08:46

Genetic Variant Detection in the CALR gene using High Resolution Melting Analysis

Published on: August 26, 2020

RBDT: A Computerized Task System based in Transposition for the Continuous Analysis of Relational Behavior Dynamics in Humans
11:09

RBDT: A Computerized Task System based in Transposition for the Continuous Analysis of Relational Behavior Dynamics in Humans

Published on: July 17, 2021

  • これらの複合体によって媒介される明確な分解経路の証拠を提供した.
  • 結論:

    • 2つの異なるタンパク質複合体は,エンドプラズマ網膜におけるタンパク質分解における基板特異性を媒介する.
    • これらの複合体は,特定の間違った折りたたまれたタンパク質の標的の除去を保証し,細胞ホメオスタシスを維持します.
    • この発見は,細胞内の複雑なタンパク質品質管理機構についての新しい洞察を提供します.