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相关概念视频

Assembly of Signaling Complexes01:30

Assembly of Signaling Complexes

6.0K
Multiprotein signaling complexes are formed in a dynamic process involving protein-protein interactions at the cytoplasmic domain of transmembrane receptors or enzymatic and non-enzymatic proteins associated with the receptor. These complexes ensure the activation and propagation of intracellular signals that regulate cell functions.
Interaction domains in cell signaling
Interaction domains recognize exposed features of their binding partners containing post-translationally modified sequences,...
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Mechanisms of Membrane Domain Formation00:59

Mechanisms of Membrane Domain Formation

3.2K
Different physical properties of lipids and proteins allow them to localize and form distinct islands or domains in the membrane. Some membrane domains are formed due to protein-protein interactions, whereas others are formed due to the presence of specific lipids such as sphingolipids and sterols—for example, large proteins, such as bacteriorhodopsin, aggregate and create distinct domains.
Another mechanism for membrane domain formation involves membrane proteins interacting with...
3.2K
Assembly of Complex Microtubule Structures01:32

Assembly of Complex Microtubule Structures

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Complex microtubule structures are present in resting cells and in dividing cells. In resting cells, they are responsible for maintaining the cellular architecture, tracks for intracellular transport, positioning of organelles, assembly of cilia and flagella. They mediate the bipolar spindle assembly for chromosomal segregation and positioning of the cell division plate in dividing cells. The formation of microtubule complex structures depends on the cell type, cell stage, and cell function.
1.9K
Protein Complex Assembly02:41

Protein Complex Assembly

11.1K
Proteins can form homomeric complexes with another unit of the same protein or heteromeric complexes with different types.  Most protein complexes self-assemble spontaneously via ordered pathways, while some proteins need assembly factors that guide their proper assembly. Despite the crowded intracellular environment, proteins usually interact with their correct partners and form functional complexes.
Many viruses self-assemble into a fully functional unit using the infected host cell to...
11.1K
Assembly of Cytoskeletal Filaments01:18

Assembly of Cytoskeletal Filaments

21.4K
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...
21.4K
Actin Polymerization and Cell Motility01:13

Actin Polymerization and Cell Motility

5.5K
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....
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相关实验视频

Updated: Sep 19, 2025

Detecting and Characterizing Protein Self-Assembly In Vivo by Flow Cytometry
05:58

Detecting and Characterizing Protein Self-Assembly In Vivo by Flow Cytometry

Published on: July 17, 2019

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膜相关自组件用于细胞决策.

Samuel L Foley1, Margaret E Johnson1

  • 1T. C. Jenkins Department of Biophysics, Johns Hopkins University, Baltimore, Maryland, USA.

ArXiv
|June 5, 2025
PubMed
概括

表面上的分子自我组装作为检测细胞受体的敏感开关. 这种被动机制为活跃的细胞信号通路提供了一个可调节和强大的替代方案.

科学领域:

  • 生物物理学的生物物理.
  • 细胞生物学 细胞生物学
  • 生物化学 生物化学

背景情况:

  • 细胞决策依赖于传递外界信号的跨膜受体.
  • 受体信号通常涉及不可逆转的,能源依赖的生化反应.
  • 现有的被动检测机制缺乏活跃途径的灵敏度.

研究的目的:

  • 研究自发分子自我组装作为用于受体检测的可调和强大的开关.
  • 将自组装机制的灵敏度与被动和活性受体检测方法进行比较.
  • 开发一个理论框架来理解基于自组装的蜂开关.

主要方法:

  • 对临界受体密度的分析表达式的导出.
  • 使用平衡静态反应-扩散模拟.
  • 将理论预测与模拟结果进行比较.

主要成果:

  • 自发的分子自我组装可以作为在生理度下检测受体的敏感开关.
  • 这种自组装机制与其他被动检测方法相比,显示出更高的灵敏度.
  • 分析表达式准确地预测了组合核和生长的关键受体密度.

结论:

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Reconstitution of Septin Assembly at Membranes to Study Biophysical Properties and Functions

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Detecting and Characterizing Protein Self-Assembly In Vivo by Flow Cytometry
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Detecting and Characterizing Protein Self-Assembly In Vivo by Flow Cytometry

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Reconstitution of Septin Assembly at Membranes to Study Biophysical Properties and Functions

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  • 分子自我组装为细胞信号检测提供了灵敏,可调和和强大的机制.
  • 开发的理论为控制决策门和响应量提供了洞察力.
  • 这种被动机制为消耗能源的主动信号通路提供了可行的替代方案.