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相关概念视频

Clathrin Coated Vesicles01:12

Clathrin Coated Vesicles

Clathrin-coated vesicles use endocytosis to transport receptors and lysosomal hydrolases from the Golgi to the lysosome in the late secretory pathway. Clathrin-mediated endocytosis was the first described endocytic process, and Clathrin-coated vesicles remain one of the most well-studied transport vesicles. The molecular machinery that generates clathrin-coated vesicles comprises over 50 proteins that precisely coordinate vesicle formation. Cell surface receptors concentrated in indented sites...
Fluid Mosaic Model01:19

Fluid Mosaic Model

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 with the analogy of...
COP Coated Vesicles00:59

COP Coated Vesicles

Membrane-enclosed structures called vesicles transport proteins and lipids across the cell. The vesicles derive their cargo from the plasma membrane, Golgi, ER, or endosome. Coated vesicles are spherical, protein-coated carriers with a 50–100 nm diameter that mediate bidirectional transport between the ER and the Golgi. The distribution of proteins between the ER and Golgi complex is dynamic and is maintained by different coated vesicles. Their formation is driven by the assembly of different...
Membrane Carbohydrates01:30

Membrane Carbohydrates

The plasma membrane is a dynamic barrier composed of lipids, proteins, and carbohydrates. It is the epicenter of many cellular processes required for cell growth and survival. Carbohydrates have unique structural and chemical properties that help the plasma membrane to carry out its functions effectively.
Membrane carbohydrates do not have any hydrophobic region and are exclusively located on the cell's outer surface. The addition of sugar molecules or glycosylation of proteins happens in...
Pinching-off of Coated Vesicles01:32

Pinching-off of Coated Vesicles

Vesicle budding is orchestrated by distinct cytosolic proteins such as adaptor proteins, coat proteins, and GTPases. To initiate vesicle budding, membrane-bending proteins containing crescent-shaped BAR domains bind to the lipid heads in the bilayer and distort the membrane to form a protein-coated vesicle bud. Adaptors proteins such as AP2 for clathrin-coated vesicles can nucleate on the deformed membrane. Finally, coat proteins such as clathrin or COPI and COPII assemble into a coat forming...

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相关实验视频

Updated: Jun 24, 2026

Lipid Vesicle-mediated Affinity Chromatography using Magnetic Activated Cell Sorting (LIMACS): a Novel Method to Analyze Protein-lipid Interaction
07:33

Lipid Vesicle-mediated Affinity Chromatography using Magnetic Activated Cell Sorting (LIMACS): a Novel Method to Analyze Protein-lipid Interaction

Published on: April 26, 2011

碳水化合物修饰的catanionic囊泡:在双层接口处探测多价值结合.

Glen B Thomas1, Lenea H Rader, Juhee Park

  • 1Department of Chemistry and Biochemistry, University of Maryland, College Park, Maryland 20742, USA.

Journal of the American Chemical Society
|March 28, 2009
PubMed
概括
此摘要是机器生成的。

研究人员合成了功能化囊泡,以研究糖分子分布如何影响蛋白质结合. 他们发现,控制这种分布会影响结合动力学,并可能导致囊泡聚合,从而提供了对界面上的分子相互作用的见解.

更多相关视频

Assembly of Cell Mimicking Supported and Suspended Lipid Bilayer Models for the Study of Molecular Interactions
12:18

Assembly of Cell Mimicking Supported and Suspended Lipid Bilayer Models for the Study of Molecular Interactions

Published on: August 3, 2021

相关实验视频

Last Updated: Jun 24, 2026

Lipid Vesicle-mediated Affinity Chromatography using Magnetic Activated Cell Sorting (LIMACS): a Novel Method to Analyze Protein-lipid Interaction
07:33

Lipid Vesicle-mediated Affinity Chromatography using Magnetic Activated Cell Sorting (LIMACS): a Novel Method to Analyze Protein-lipid Interaction

Published on: April 26, 2011

Assembly of Cell Mimicking Supported and Suspended Lipid Bilayer Models for the Study of Molecular Interactions
12:18

Assembly of Cell Mimicking Supported and Suspended Lipid Bilayer Models for the Study of Molecular Interactions

Published on: August 3, 2021

科学领域:

  • 超分子化学 超分子化学
  • 生物物理化学 生物物理化学
  • 材料科学 材料科学 材料科学

背景情况:

  • 了解界面上的分子相互作用对于开发先进材料和药物输送系统至关重要.
  • 囊泡表面的连接体的空间布局影响它们与多价值蛋白质的结合.
  • 卡塔尼克囊泡为研究这些界面现象提供了一个可调的平台.

研究的目的:

  • 合成和表征表面功能化,负电荷的catanionic囊泡.
  • 为了研究甘氨酸结合物分布对莱克结合动学的影响.
  • 探索连接体分离距离和多价值结合事件之间的关系.

主要方法:

  • 表面功能化的catanionic囊泡的合成和表征.
  • 使用O结合和N结合的葡萄糖合物与莱克的结合性研究.
  • 低温传导电子显微镜 (cryo-TEM) 用于形态分析.

主要成果:

  • 通过改变化学结构,可以控制囊泡膜中的糖合物分布.
  • O-联结结合体显示了非相互作用的联结体结合动力学,而N-联结结合体显示了相互作用或聚类联结体.
  • 低温TEM显示,在与康卡纳瓦林A聚合时,囊泡多层,这取决于连接体密度.

结论:

  • 对囊泡表面的受控联体分布允许研究多价值结合相互作用.
  • 这些发现提供了一种方法来确定有效的结合点分离和关键连接体密度.
  • 表面功能化囊泡对研究基本的结合现象和材料自组装具有前景.