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

Chemotaxis and Direction of Cell Migration01:21

Chemotaxis and Direction of Cell Migration

5.9K
Cells can detect chemical cues in their environment and reorganize the cytoskeleton to migrate toward them or away from them. This directional migration, called chemotaxis, is essential during embryogenesis and development, immune response, tissue repair and regeneration, and reproduction. These chemical cues can either attract or repel the cell's movement. For example, axon development is determined by a combination of chemoattractants and chemorepellents that direct the growing axon...
5.9K
Chemotaxis in E. coli01:27

Chemotaxis in E. coli

1.0K
Chemotaxis in Escherichia coli is a sensory-driven motility mechanism that enables bacteria to navigate chemical gradients, moving toward beneficial environments while avoiding harmful conditions. This process relies on a signal transduction system integrating external chemical cues with flagellar motor control.Chemoreceptors and Signal DetectionE. coli detects chemical gradients through methyl-accepting chemotaxis proteins (MCPs), which are membrane-bound chemoreceptors that sense attractants...
1.0K
Separation of Sister Chromatids02:17

Separation of Sister Chromatids

4.6K
At the transition from prophase to metaphase, there is a reduction in cohesion along the chromosomal arms, resulting in the resolution of sister chromatids. However, residual cohesin connections remain to hold the sister chromatids together until the transition from metaphase to anaphase. The residual connection prevents any premature separation of sister chromatids, blocking the risks of aneuploidy within the daughter cells.
At the onset of anaphase, separase, a proteolytic enzyme, is...
4.6K
Cell Migration01:09

Cell Migration

18.9K
Cell migration, the process by which cells move from one location to another, is essential for the proper development and viability of organisms throughout their life. When cells are not able to migrate properly to their ordained locations, various disorders may occur. For example, disruption in cell migration causes chronic inflammatory diseases such as arthritis.
18.9K
Mechanism of Lamellipodia Formation01:31

Mechanism of Lamellipodia Formation

3.8K
Cells migrating in response to external stimuli form lamellipodia, which are thin membrane protrusions supported by a mesh of linked, branched, or unbranched actin filaments. These actin filaments interact with myosin motor proteins, creating the dynamic actomyosin complex within the cytoskeleton. Contractility, or the ability to generate contractile stress, is inherent to the actomyosin complex. It helps cells detect the stiffness of the surrounding ECM and exert contractile force for...
3.8K
Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

6.4K
DNA replication is initiated at sites containing predefined DNA sequences known as origins of replication. DNA is unwound at these sites by the minichromosome maintenance (MCM) helicase and other factors such as Cdc45 and the associated GINS complex.The unwound single strands are protected by replication protein A (RPA) until DNA polymerase starts synthesizing DNA at the 5’ end of the strand in the same direction as the replication fork. To prevent the replication fork from falling apart,...
6.4K

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

Lévy Diffusion Under Power-Law Stochastic Resetting.

Entropy (Basel, Switzerland)·2026
Same author

Orientation-Modulated Hyperuniformity in Frustrated Vicsek-Kuramoto Systems.

Entropy (Basel, Switzerland)·2026
Same author

Visual quorum sensing in chiral suspensions: Hyperuniformity and edge currents.

PNAS nexus·2025
Same author

Artificial neurons made of active matter memristors.

Soft matter·2025
Same author

Ratcheting by Stochastic Resetting With Fat-Tailed Time Distributions.

Chemphyschem : a European journal of chemical physics and physical chemistry·2024
Same author

Autonomous ratcheting by stochastic resetting.

The Journal of chemical physics·2023
Same journal

Revisiting crossed-correlated baths in open quantum systems simulated by HEOM or T-TEDOPA.

The Journal of chemical physics·2026
Same journal

Vesicle size and membrane composition control monomer transfer pathways in multicomponent lipid vesicles.

The Journal of chemical physics·2026
Same journal

Polaron-mediated exciton dynamics of P(NDI2OD-T2) unveiled by transient absorption spectroscopy under electrochemical conditions.

The Journal of chemical physics·2026
Same journal

Green-Kubo relation in a mesoscale odd fluid model.

The Journal of chemical physics·2026
Same journal

Nitrogenation of microscopic MoS2 surfaces by oxidation scanning probe lithography.

The Journal of chemical physics·2026
Same journal

Molecular structure, binding, and disorder in TDBC-Ag plexcitonic assemblies.

The Journal of chemical physics·2026
查看所有相关文章

相关实验视频

Updated: Feb 24, 2026

Assessment of Dictyostelium discoideum Response to Acute Mechanical Stimulation
10:40

Assessment of Dictyostelium discoideum Response to Acute Mechanical Stimulation

Published on: November 9, 2017

7.4K

由化学反应缺陷引发的活性相分离.

Yujuan Song1, Feifei Liu1, Qingqing Yin1

  • 1MOE Key Laboratory of Advanced Micro-Structured Materials, School of Physics Science and Engineering, Tongji University, Shanghai 200092, China.

The Journal of chemical physics
|February 23, 2026
PubMed
概括
此摘要是机器生成的。

活性悬浮中的缺陷迅速触发颗粒聚合,使运动诱导相分离 (MIPS) 即使在低密度下. 这种机制可以解释细菌生物膜的形成.

更多相关视频

Traction Microscopy Integrated with Microfluidics for Chemotactic Collective Migration
10:53

Traction Microscopy Integrated with Microfluidics for Chemotactic Collective Migration

Published on: October 13, 2019

7.5K
Imaging G Protein-coupled Receptor-mediated Chemotaxis and its Signaling Events in Neutrophil-like HL60 Cells
08:24

Imaging G Protein-coupled Receptor-mediated Chemotaxis and its Signaling Events in Neutrophil-like HL60 Cells

Published on: September 14, 2016

10.6K

相关实验视频

Last Updated: Feb 24, 2026

Assessment of Dictyostelium discoideum Response to Acute Mechanical Stimulation
10:40

Assessment of Dictyostelium discoideum Response to Acute Mechanical Stimulation

Published on: November 9, 2017

7.4K
Traction Microscopy Integrated with Microfluidics for Chemotactic Collective Migration
10:53

Traction Microscopy Integrated with Microfluidics for Chemotactic Collective Migration

Published on: October 13, 2019

7.5K
Imaging G Protein-coupled Receptor-mediated Chemotaxis and its Signaling Events in Neutrophil-like HL60 Cells
08:24

Imaging G Protein-coupled Receptor-mediated Chemotaxis and its Signaling Events in Neutrophil-like HL60 Cells

Published on: September 14, 2016

10.6K

科学领域:

  • 物理 物理学 物理
  • 软物质物理学 软物质物理学
  • 生物物理学的生物物理.

背景情况:

  • 运动诱导相分离 (MIPS) 是活性物质的一个关键现象.
  • 在低粒子密度 (双节区域) 中实现MIPS在计算上具有挑战性.
  • 现有的模型往往需要高的包装分数或长时间的模拟时间.

研究的目的:

  • 研究一种在稀释剂中快速MIPS的新机制.
  • 探索故障在启动和驾驶阶段分离中的作用.
  • 提供对生物聚合过程的见解,例如生物膜形成.

主要方法:

  • 活跃悬浮的数值模拟.
  • 分析缺陷动态及其对粒子聚合的影响.
  • 改变初始条件和系统参数以研究由缺陷触发的MIPS.

主要成果:

  • 缺陷充当有效的化学反应中心,迅速形成局部粒子聚合物.
  • 这些聚合物可以生长和凝聚,导致完全相位分离.
  • 缺陷触发机制显著降低了双节区域MIPS的时间和计算成本.

结论:

  • 缺陷诱导的聚合在低密度下为MIPS提供了一条有效的途径.
  • 这种机制为细菌聚合成生物膜提供了潜在的解释.
  • 营养素颗粒可以作为化疗吸引剂,类似于物理模型中的缺陷.