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相关概念视频

Mechanism of Filopodia Formation01:39

Mechanism of Filopodia Formation

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Filopodia are thin, actin-rich cellular protrusions that play an important role in many fundamental cellular functions. They vary in their occurrence, length, and positioning in different cell types, suggesting their diverse roles.
Their main function is to guide migrating cells during normal tissue morphogenesis or cancer metastasis by recognizing and making initial contacts with the extracellular matrix. However, they can also act as stationary cell anchors or help to establish communication...
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Mechanism of Lamellipodia Formation01:31

Mechanism of Lamellipodia Formation

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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...
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Mechanism of Ciliary Motion01:05

Mechanism of Ciliary Motion

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The ciliary structures were first seen in 1647 by Antonie Leeuwenhoek while observing the protozoans. In lower organisms, these appendages are responsible for cell movement, while in higher organisms, these appendages help in the movement of the extracellular fluids within the body cavities.
The cilia are made up of microtubules in a 9+2 arrangement, with nine microtubule doublet ring bundles, surrounding a pair of central singlet microtubule bundles. The doublet microtubule bundles are...
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Microtubules in Cell Motility01:24

Microtubules in Cell Motility

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Microtubules are thick hollow cylindrical proteins that help form the cytoskeleton. Microtubules have varied roles in the cell. These filaments help form cellular appendages like cilia and flagella, which are responsible for locomotion. The cilia arise from basal bodies, separated from the main body by a membrane-like structure forming the transition zone. This zone is the gate for the entry of lipids and proteins, creating a unique composition of lipids and proteins in the ciliary membrane and...
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Microtubule Associated Motor Proteins01:32

Microtubule Associated Motor Proteins

7.8K
Eukaryotic cells have different motor proteins for transporting various cargo within the cell. These motor proteins differ based on the filament they associate with, the direction they move within the cell, and the type of cargo they transport. Motor proteins that associate with microtubules are known as microtubule-associated motor proteins. There are two families of microtubule-associated motor proteins —Kinesins and Dyneins. Both these proteins assist in the transport of cellular...
7.8K
Coat Assembly and GTPases01:33

Coat Assembly and GTPases

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Vesicles incorporate different coat protein subunits in different cell locations, which changes the properties of the coat, such as the shape and geometry of the transport vesicles. Thus, vesicle coat proteins also play a significant role in cargo selection.
Coat assembly depends on the local availability of phosphatidylinositol phosphates or PIPs and GTP-binding proteins. Adaptor proteins, which link the coat proteins to the membrane, bind to these PIPs and play a crucial role in controlling...
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相关实验视频

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Biophysical Characterization of Flagellar Motor Functions
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Biophysical Characterization of Flagellar Motor Functions

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在Tad pilus系统电机CpaF中双向的柱子处理.

Michael Hohl1, Emma J Banks2, Max P Manley1

  • 1Department of Infectious Disease, Imperial College, London, UK.

Nature communications
|August 5, 2024
PubMed
概括

细菌紧固粘附柱体系统 (TadPS) ATPase CpaF (TadA) 驱动柱体延伸和收缩. 这项研究揭示了CpaF.

科学领域:

  • 微生物学 微生物学
  • 结构生物学 结构生物学
  • 生物化学 生物化学

背景情况:

  • 细菌紧固粘附柱状系统 (TadPS) 对于病原体的粘附和殖民至关重要.
  • 柱子的组装和动态是由ATPase CpaF (TadA) 驱动的,但它的机制仍然不清楚.

研究的目的:

  • 阐明CpaF (TadA) 在驱动TadPS柱体动态中的分子机制.
  • 描述CpaF的ATPase活性和形状变化的结构基础.

主要方法:

  • 低温电子显微镜 (cryo-EM) 用于确定不同核酸状态中的CpaF结构.
  • 基于细胞的光显微镜来评估CpaF突变的体内功能.
  • 生物化学试验用于研究核酸循环和形状变化.

主要成果:

  • CpaF (TadA) 形成一个具有C2对称性的六合体,经历核酸依赖的构造变化.
  • 核酸循环涉及一个子单元内部的状机制,驱动着连续的子单元变化.
  • 突变分析确定了参与CpaF与平台蛋白相互作用的关键残留物 (CpaG/TadB,CpaH/TadC).

结论:

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Application of High-speed Super-resolution SPEED Microscopy in Live Primary Cilium
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Application of High-speed Super-resolution SPEED Microscopy in Live Primary Cilium

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Application of High-speed Super-resolution SPEED Microscopy in Live Primary Cilium
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  • 提出了一个CpaF (TadA) 驱动的双向柱状运动模型.
  • 了解CpaF机制,可以了解更广泛的4型光纤组装ATPases家族.
  • 这项工作对准人类病原体中的细菌粘附机制有影响.