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相关概念视频

Translocation of Proteins into the Mitochondria01:19

Translocation of Proteins into the Mitochondria

3.1K
Mitochondrial precursors are translocated to the internal subcompartments via independent mechanisms involving distinct protein machineries called translocases.
Sorting of outer membrane proteins:
Mitochondrial outer membrane proteins are of two types: the transmembrane, beta-barrel porins, and the membrane-anchored, alpha-helical proteins. Beta-barrel porin precursors are translocated by the TOM complex and inserted into the outer mitochondrial membrane by the SAM complex. In contrast,...
3.1K
Cotranslational Protein Translocation01:20

Cotranslational Protein Translocation

7.3K
Translocation of proteins across membranes is an ancient process that occurs even in bacteria and archaebacteria. In fact, the components of the translocation machinery are still conserved between prokaryotes and eukaryotes.
Sec61 channel partners for cotranslational translocation
During cotranslational translocation, the Sec61 channel partners with the signal recognition particle (SRP), the signal recognition particle receptor (SR), and the ribosomes to transport the nascent polypeptide chain...
7.3K
Protein Transport to the Thylakoids01:22

Protein Transport to the Thylakoids

2.3K
Thylakoids are membrane-bound sac-like structures within the chloroplast that serve as sites for photosynthesis. Thylakoid lumen contains many electron transport proteins and is enclosed by a thylakoid membrane rich in the light-harvesting complex. Proteins targeted to the thylakoids are transported as precursors and are sorted by the general TOC/TIC import pathway. Once the precursor reaches the stroma, stromal processing peptidases remove their transit signal and expose thylakoid signal...
2.3K
Energy to Drive Translocation01:37

Energy to Drive Translocation

2.1K
Mitochondrial protein import is powered by two distinct energy sources: ATP hydrolysis and electrochemical potential across the inner membrane. Newly synthesized precursors are bound by cytosolic chaperones of the Hsp70 family, which guide them to the import receptors on the mitochondrial surface. Utilizing the energy of ATP hydrolysis, Hsp70 chaperones transfer these precursors to the TOM receptors on the mitochondrial outer membrane.
Generally, polypeptides are unfolded by two distinct...
2.1K
Protein Transport into the Inner Mitochondrial Membrane01:34

Protein Transport into the Inner Mitochondrial Membrane

3.7K
Nuclear encoded mitochondrial precursors are imported to the inner membrane in a multistep process involving two separate translocons, TIM22 and TIM23. TIM23 is a cation-selective pore that remains closed by the N terminal segment of the protein. Negative charges on the TIM23 act as a receptor for the incoming precursor, pulling the positively charged matrix-targeting sequence for peptide insertion and translocation.
Transport of mitochondrial precursors across the TIM23 channel is driven by...
3.7K
Protein Translocation Machinery on the ER Membrane01:28

Protein Translocation Machinery on the ER Membrane

4.6K
The translocon complex situated on the ER membrane is the main gateway for the protein secretory pathway. It facilitates the transport of nascent peptides into the ER lumen and their insertion into the ER membrane.
Sec61 protein conducting channel
In eukaryotes, the translocon complex comprises a core heterotrimeric translocator channel called the Sec61 complex. This channel includes three transmembrane proteins, Sec61α, Sec61β, and Sec61γ, and is the largest subunit of the...
4.6K

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相关实验视频

Updated: Jul 1, 2025

Detection of Toxin Translocation into the Host Cytosol by Surface Plasmon Resonance
10:41

Detection of Toxin Translocation into the Host Cytosol by Surface Plasmon Resonance

Published on: January 3, 2012

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炭毒素:研究蛋白质转位的模型系统

Bryan A Krantz1

  • 1Department of Microbial Pathogenesis, School of Dentistry, University of Maryland, Baltimore, 650 W. Baltimore Street, Baltimore, MD 21201, USA.

Journal of molecular biology
|March 8, 2024
PubMed
概括

人类炭毒素的毒素.

科学领域:

  • 生物物理学的生物物理.
  • 分子生物学分子生物学
  • 生物化学 生物化学

背景情况:

  • 转位酶通道是分子机器,它在膜上展开和转位蛋白质.
  • 由于折叠的蛋白质的热力学稳定性,蛋白质的展开和转移需要能量.
  • 片的活性部位通常被转位酶通道利用以催化展开.

研究的目的:

  • 用炭毒素作为生物物理模型系统来研究蛋白质转位.
  • 阐明炭毒素保护抗原 (PA) 通道促进蛋白质展开和转移的机制.
  • 将炭毒素转位机制与其他已知的转位酶通道进行比较.

主要方法:

  • 使用炭毒素,特别是保护性抗原 (PA),作为模型转位酶通道.
  • 研究了片位 (α,φ,充电) 在PA通道中的作用.
  • 研究了内体质子梯度对蛋白质展开和转位的影响.
  • 分析了两种由质子梯度驱动的转位模型:布朗式杆和螺旋式压缩机制.

主要成果:

  • 炭毒素的保护性抗原 (PA) 作为一个寡合转位酶通道.
  • 在PA通道内的三个片位催化了展开和转位.
  • 内体质子梯度为展开和转位过程提供动力.
关键词:
布朗的拉切特 布朗的拉切特酸紧固件的使用方法动力冲击 动力冲击 动力冲击质子梯度的梯度 质子梯度转位道的转位道

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A Simple Fluorescence-based Reporter Assay to Identify Cellular Components Required for Ricin Toxin A Chain RTA Trafficking in Yeast
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A Simple Fluorescence-based Reporter Assay to Identify Cellular Components Required for Ricin Toxin A Chain RTA Trafficking in Yeast

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Analyzing Dynamic Protein Complexes Assembled On and Released From Biolayer Interferometry Biosensor Using Mass Spectrometry and Electron Microscopy
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Analyzing Dynamic Protein Complexes Assembled On and Released From Biolayer Interferometry Biosensor Using Mass Spectrometry and Electron Microscopy

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相关实验视频

Last Updated: Jul 1, 2025

Detection of Toxin Translocation into the Host Cytosol by Surface Plasmon Resonance
10:41

Detection of Toxin Translocation into the Host Cytosol by Surface Plasmon Resonance

Published on: January 3, 2012

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A Simple Fluorescence-based Reporter Assay to Identify Cellular Components Required for Ricin Toxin A Chain RTA Trafficking in Yeast
09:03

A Simple Fluorescence-based Reporter Assay to Identify Cellular Components Required for Ricin Toxin A Chain RTA Trafficking in Yeast

Published on: December 15, 2017

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Analyzing Dynamic Protein Complexes Assembled On and Released From Biolayer Interferometry Biosensor Using Mass Spectrometry and Electron Microscopy
09:30

Analyzing Dynamic Protein Complexes Assembled On and Released From Biolayer Interferometry Biosensor Using Mass Spectrometry and Electron Microscopy

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  • 布朗的拉切和螺旋压缩机制可能在不同的蛋白质二次结构 (分别是β-片和α-螺旋) 上运行.
  • 结论:

    • 炭毒素为研究蛋白质转位的基本原理提供了一个有价值的模型.
    • 片位和质子梯度能量的合作行动推动了高效的蛋白质转移.
    • 对于转位酶通道内的不同蛋白质二次结构,可以采用不同的转位机制.