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相关概念视频

Amyloid Fibrils03:03

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Amyloid fibrils are aggregates of misfolded proteins.  Under most circumstances, misfolded proteins are either refolded by chaperone proteins or degraded by the proteasome. However, in the case of a mutation or a disease, these proteins can accumulate to form large clusters and often further assemble to form elongated fibers, called fibrils. 
Amyloid deposits were observed as early as 1639 in the liver and the spleen.   In 1854, Rudolph Virchow performed iodine staining,...
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Divergence and Curl of Electric Field01:25

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The divergence of a vector is a measure of how much the vector spreads out (diverges) from a point. For example, an electric field vector diverges from the positive charge and converges at the negative charge. The divergence of an electric field is derived using Gauss's law and is equal to the charge density divided by the permittivity of space. Mathematically, it is expressed as
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Formation of Higher-order Actin Filaments01:11

Formation of Higher-order Actin Filaments

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The polymerization of G-actin monomers into filamentous F-actin is a multi-step process. Once the F-actins are formed, they can bundle together in different arrangements to form higher-order networks and regulate cellular functions. Common examples include the formation of lamellipodia and filopodia at the cell's leading edge by actin reorganization in a migrating cell. The microvilli on the brush border epithelial cells are also formed through the F-actin network.
The high-order actin...
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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...
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Fluid Mosaic Model01:19

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Scientists identified the plasma membrane in the 1890s and its principal chemical components (lipids and proteins) by 1915. The model for plasma membrane structure, proposed in 1935 by Hugh Davson and James Danielli, was the first model to be widely accepted in the scientific community. The model was based on the plasma membrane's "railroad track" appearance in early electron micrographs. Davson and Danielli theorized that the plasma membrane's structure resembled a sandwich...
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The fluid mosaic model was first proposed as a visual representation of research observations. The model comprises the composition and dynamics of membranes and serves as a foundation for future membrane-related studies. The model depicts the structure of the plasma membrane with a variety of components, which include phospholipids, proteins, and carbohydrates. These integral molecules are loosely bound, defining the cell’s border and providing fluidity for optimal function.
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Finite Element Modelling of a Cellular Electric Microenvironment
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在光纤捆模型中的雪崩形状.

Narendra Kumar Bodaballa1, Soumyajyoti Biswas1, Parongama Sen2

  • 1Department of Physics, <a href="https://ror.org/013vs5h31">SRM University AP</a>, Amaravati 522240, Andhra Pradesh, India.

Physical review. E
|August 20, 2024
PubMed
概括

纤维捆模型中的雪崩不对称性预测了关键故障. 随着临界点在准静态负荷下接近,雪崩形状变得对称,为材料分解提供了前体.

科学领域:

  • 物理 物理学 物理
  • 材料科学 材料科学 材料科学
  • 统计力学 统计力学

背景情况:

  • 无序的固体表现出复杂的失效行为.
  • 纤维束模型是研究材料分解的关键框架.
  • 了解雪崩动态对于预测材料故障至关重要.

研究的目的:

  • 在光纤捆模型中调查雪崩的时间演变.
  • 在不同的加载协议下识别关键故障的前体.
  • 分析加载协议对雪崩形状对称性的影响.

主要方法:

  • 在准静态和离散负载下模拟光纤束模型.
  • 雪崩时间形状和不对称性的分析.
  • 对雪崩不对称性的普遍缩放定律的推导.

主要成果:

  • 在准静态负载下,雪崩不对称性随着临界点的接近而普遍减少 (A∼(σ-σ_{c}) ^{θ}, θ≈0.25).
  • 这种不对称度量是即将发生的故障的前兆,独立于系统失调.
  • 在离散负荷下,雪崩形状保持不对称,即使在平均场极限.

结论:

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  • 雪崩形状的不对称性是对无序固体接近临界失效的强有力的指标.
  • 装载协议显著影响了雪崩的动态和可预测性.
  • 这些发现为材料故障的统计力学提供了洞察力.