Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Cytoskeletal Proteins in Bacteria01:29

Cytoskeletal Proteins in Bacteria

3.4K
Bacterial cells were initially considered simple, randomly organized structures lacking a cytoskeleton. However, the discovery of cytoskeleton homologs in bacteria led to the change of this opinion. Bacterial cytoskeletal filaments regulate the cell shape, cell polarity, cell division, and partitioning of plasmids during cell division. It was later discovered that bacterial cytoskeletal proteins, mainly actin and tubulin homologs, are diverse compared to their eukaryotic counterparts. On the...
3.4K
Assembly of Cytoskeletal Filaments01:18

Assembly of Cytoskeletal Filaments

20.5K
Cytoskeletal filaments are polymeric forms of smaller protein subunits. However, individual cytoskeletal filaments may easily disassemble or associate with other similar filaments to form rigid structures. Microfilaments, made of actin monomers, rely on actin-binding proteins to form bundles and create networks of individual actin filaments. Microtubules rely on microtubule-associated proteins (MAPs) to form sturdy cylindrical structures. However, the proteins involved in forming complex...
20.5K
Destabilization of Microtubules01:45

Destabilization of Microtubules

2.7K
The destabilization of microtubules can occur during different stages of the microtubule lifecycle, such as nucleation or elongation. It can take place at either end of the microtubule or in the microtubule lattices as a whole. The lifespan of individual microtubules within a cell varies according to the cell type and stage of the cell cycle. During interphase, the lifespan of the microtubule is about 30 minutes, while during cell division, it is about 15 minutes. In axonal microtubules of...
2.7K
Structural Protein Function01:56

Structural Protein Function

27.7K
Structural proteins are a category of proteins responsible for functions ranging from cell shape and movement to providing support to major structures such as bones, cartilage, hair, and muscles. This group includes proteins such as collagen, actin, myosin, and keratin.
Collagen, the most abundant protein in mammals, is found throughout the body. In connective tissue, such as skin, ligaments, and tendons, it provides tensile strength and elasticity.  In bones and teeth, it mineralizes to...
27.7K
Actin Filament Depolymerization01:19

Actin Filament Depolymerization

3.1K
Actin filaments (F-actin) are composed of actin subunits. The dissociation of actin monomers can occur from either end of F-actin. The rate of dissociation is faster from the minus-end or the pointed end, where the actin subunits exist with a bound ADP, together known as ADP-actin. The depolymerization of F-actin is aided by proteins, including the actin-depolymerizing factor (ADF) and cofilin family of proteins, gelsolin, and glia maturation factor (GMF).
In F-actin, the ADF/cofilin proteins...
3.1K
Intracellular Movement of Viruses and Bacteria01:10

Intracellular Movement of Viruses and Bacteria

2.8K
Intracellular bacteria and viruses often comprise a group of highly infectious pathogens that can cause several diseases. Bacterial pathogens include those belonging to the genus Rickettsia responsible for conditions such as rocky mountain spotted fever and the Mediterranean spotted fever; Chlamydia, a genus responsible for a sexually transmitted disease; Coxiella burnetii, an agent responsible for Q fever. Viral pathogens include vaccinia—a poxvirus, and herpes simplex virus—a...
2.8K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Condition-Specific Protocols Used in the Emergency Department Observation Unit: A Scoping Review.

Journal of the American College of Emergency Physicians open·2026
Same author

Stress-Responsive Protein IFRD1 Protects Assembled Ribosomes via a Ribosome-Salvaging Mechanism.

bioRxiv : the preprint server for biology·2026
Same author

Luminal epithelium remodeling underlies endometrial regeneration during menstruation and pregnancy.

bioRxiv : the preprint server for biology·2026
Same author

Induction of menstruation in mice reveals the regulation of menstrual shedding.

bioRxiv : the preprint server for biology·2025
Same author

ATP-dependent actin barbed-end fluctuations at steady state.

Proceedings of the National Academy of Sciences of the United States of America·2025
Same author

The 21st century marks a rise in TURP retreatment rates: an analysis of Veterans Health Administration data.

World journal of urology·2025

相关实验视频

Updated: Jul 9, 2025

Visualization of Bacterial Toxin Induced Responses Using Live Cell Fluorescence Microscopy
14:29

Visualization of Bacterial Toxin Induced Responses Using Live Cell Fluorescence Microscopy

Published on: October 1, 2012

12.0K

重温细菌细胞杀伤性扩张毒素的结构和功能.

Henry Chen1, Claire J Ang1, Molly K Crowder1

  • 1Department of Microbiology, School of Molecular and Cellular Biology, University of Illinois at Urbana-Champaign, Urbana, IL, United States.

Frontiers in cellular and infection microbiology
|November 30, 2023
PubMed
概括
此摘要是机器生成的。

细胞杀伤性扩散毒素 (CDT) 需要特定的子单元来进行宿主细胞活动. 这项研究表明,功能性的Campylobacter jejuni CDT (Cj-CDT) 不需要预组装的异构分离剂,挑战现有模型.

关键词:
这是一种AB毒素.坎比洛巴克特 (Campylobacter jejuniuni) 是一个常见的菌类.造成的DNA损伤是DNA损伤.细胞杀伤性扩散毒素整毒素结构结构 整毒素结构结构蛋白质与蛋白质的相互作用

更多相关视频

Applying Live Cell Imaging and Cryo-Electron Tomography to Resolve Spatiotemporal Features of the Legionella pneumophila Dot/Icm Secretion System
09:12

Applying Live Cell Imaging and Cryo-Electron Tomography to Resolve Spatiotemporal Features of the Legionella pneumophila Dot/Icm Secretion System

Published on: March 10, 2020

7.0K
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

13.4K

相关实验视频

Last Updated: Jul 9, 2025

Visualization of Bacterial Toxin Induced Responses Using Live Cell Fluorescence Microscopy
14:29

Visualization of Bacterial Toxin Induced Responses Using Live Cell Fluorescence Microscopy

Published on: October 1, 2012

12.0K
Applying Live Cell Imaging and Cryo-Electron Tomography to Resolve Spatiotemporal Features of the Legionella pneumophila Dot/Icm Secretion System
09:12

Applying Live Cell Imaging and Cryo-Electron Tomography to Resolve Spatiotemporal Features of the Legionella pneumophila Dot/Icm Secretion System

Published on: March 10, 2020

7.0K
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

13.4K

科学领域:

  • 微生物学 微生物学
  • 分子生物学分子生物学
  • 毒理学 毒理学 毒理学

背景情况:

  • 细胞杀伤性扩散毒素 (CDT) 是由病原体产生的细菌基因毒素.
  • CDT通过与血膜结合来向宿主细胞.
  • 据认为,最大的CDT活动需要预组装的CdtA,CdtB和CdtC子单元的三方复合体.

研究的目的:

  • 实验性研究Campylobacter jejuni CDT (Cj-CDT) 的亚单元相互作用和细胞活性之间的关系.
  • 为了确定预组装的异体合物复合物是否对于Cj-CDT的基因毒性作用是必要的.

主要方法:

  • 同免疫沉和透析保留试验用于检测异体合物复合物.
  • 微尺度热泳以评估子单元相互作用亲和力.
  • 细胞循环停止试验测量在G2/M接口上测量毒素活性.

主要成果:

  • 只有在非常高的亚单元度下才检测到异构三体Cj-CDT复合体.
  • 在Cj-CDT子单元之间观察到低亲和度相互作用.
  • 毒素介导的细胞循环停止发生在子单元度显著低于形成异构分离体的水平.

结论:

  • 被广泛接受的CDT作为预组装的异构分离剂的模型受到这些发现的挑战.
  • 在有效度下,Cj-CDT可能作为不相互作用的子单元的混合物起作用.
  • 需要进一步的研究来阐明CDT中毒的确切机制.