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相关概念视频

Actin Polymerization and Cell Motility01:13

Actin Polymerization and Cell Motility

7.1K
Actin is a family of globular proteins that are highly abundant in eukaryotic cells. It makes up approximately 1-5% of total cell protein concentration. Actin monomers polymerize to form a complex network of polarized filaments, the actin cytoskeleton, that plays a crucial role in many cellular processes, including cell motility, division, endocytosis, and metastasis of cancer cells.
Actin cytoskeleton dynamics can produce pushing, pulling, and resistance forces that help the cell to migrate....
7.1K
Actin Polymerization01:42

Actin Polymerization

8.9K
Actin polymerization occurs through the head-to-tail association of binding sites on monomeric actin or G-actin to form filamentous or F-actin. The polymerization can be divided into three phases ̶  nucleation, elongation, and steady-state phase.
The nucleation phase involves forming a stable nucleus consisting of three actin monomers to form a new actin filament. Actin-binding proteins such as formins and Arp2/3 complex help filament growth post-nucleation. The Formins form straight...
8.9K
Generation of Straight or Branched Actin Filaments01:14

Generation of Straight or Branched Actin Filaments

4.0K
The straight or branched structure formation of actin filaments is controlled by nucleating proteins such as the formins and Arp2/3 complex. Formin-mediated assembly results in straight filaments, whereas Arp2/3 protein complex-mediated assembly results in branched actin filaments.
Arp2/3 Complex
Arp2/3 complex is a seven-subunit complex consisting of two proteins similar to actin- Arp2 and Arp3, and five other subunits that help keep Arp2 and Arp3 inactive. When required, the complex is...
4.0K
Actin Filament Depolymerization01:19

Actin Filament Depolymerization

4.1K
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...
4.1K
Introduction to Actin01:26

Introduction to Actin

6.9K
Actin is a highly conserved cytoskeletal protein found abundantly in eukaryotic cells. It constitutes 10% weight of the total cellular protein in muscle cells, while in non-muscle cells, it is lower and makes up around 1–5 percent of the total cell protein. Actin found in the unicellular amoebae and complex multicellular animals is around 80% similar, demonstrating their conservation over a billion years of evolution.  Actin coding genes are conserved within species and across...
6.9K
The Role of Actin and Myosin in Non-muscle Cells01:10

The Role of Actin and Myosin in Non-muscle Cells

5.6K
Actin and myosin or actomyosin filaments also play a significant role in cells other than those involved in muscle contraction (which occurs within the sarcomere of muscle cells). The mechanism of non-muscle cell contractile bundles was first observed in Dictyostelium and Acanthamoeba. In non-muscle cells, two bundles are commonly found: stress fibers and actomyosin adherence belts. These contractile bundles are smaller and less organized than the ones found in muscle cells. They  are held...
5.6K

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相关实验视频

Updated: Mar 18, 2026

Tuning the Contractility and Deformation Modes of Active Actin-Based Assemblies In Vitro: From Two-Dimensional Active Networks to Liquid Crystal Drops
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Tuning the Contractility and Deformation Modes of Active Actin-Based Assemblies In Vitro: From Two-Dimensional Active Networks to Liquid Crystal Drops

Published on: July 11, 2025

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没有Actin的执行器

Anja Geitmann1

  • 1Department of Plant Science, Faculty of Agricultural and Environmental Sciences, McGill University, Macdonald Campus, 21111 Lakeshore, Ste-Anne-de-Bellevue, QE H9X 3V9, Canada.

Cell
|July 2, 2016
PubMed
概括
此摘要是机器生成的。

卡尔达种子通过水果的开口爆炸性地分散. 这种植物机械作用是由压调节和细胞壁特性结合而来的.

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Aip1p Dynamics Are Altered by the R256H Mutation in Actin
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Reconstitution of Actin-Based Motility with Commercially Available Proteins
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Reconstitution of Actin-Based Motility with Commercially Available Proteins

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相关实验视频

Last Updated: Mar 18, 2026

Tuning the Contractility and Deformation Modes of Active Actin-Based Assemblies In Vitro: From Two-Dimensional Active Networks to Liquid Crystal Drops
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Tuning the Contractility and Deformation Modes of Active Actin-Based Assemblies In Vitro: From Two-Dimensional Active Networks to Liquid Crystal Drops

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Aip1p Dynamics Are Altered by the R256H Mutation in Actin
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Aip1p Dynamics Are Altered by the R256H Mutation in Actin

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Reconstitution of Actin-Based Motility with Commercially Available Proteins
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科学领域:

  • 植物生物力学
  • 植物繁殖

背景情况:

  • 植物利用器官运动的执行器,使其能够对环境刺激和机械功能做出反应.
  • 种子分散是植物繁殖和生存的关键方面.

研究的目的:

  • 为了研究卡尔达明花的爆炸性种子散布的生物机械机制.
  • 了解流调节和细胞壁特性在水果开口中的相互作用.

主要方法:

  • 对卡尔达花开花的观察研究.
  • 果细胞内流调节的分析.
  • 在果实脱落过程中评估细胞壁的机械性质.

主要成果:

  • 卡尔达果的爆炸性开口被证实是种子的分散机制.
  • 突压力变化和细胞壁的机械特性之间的复杂相互作用被确定为驱动力.
  • 发现特定的细胞壁特性对快速和强烈的果实分裂至关重要.

结论:

  • 这项研究阐明了 Cardamine hirsuta 用于种子散播的复杂生物机械策略.
  • 突调节和细胞壁机制是这种物种爆炸性果实开放的关键决定因素.
  • 了解这些机制可以了解植物适应和生殖的进化策略.