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相关概念视频

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...
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...
Coat Assembly and GTPases01:33

Coat Assembly and GTPases

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...
Mechanism of Filopodia Formation01:39

Mechanism of Filopodia Formation

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...
Mechanism of Lamellipodia Formation01:31

Mechanism of Lamellipodia Formation

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...
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...

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相关实验视频

Updated: May 7, 2026

In vivo and in vitro Studies of Adaptor-clathrin Interaction
17:14

In vivo and in vitro Studies of Adaptor-clathrin Interaction

Published on: January 27, 2011

克拉特林涂层坑的曲率是由epsin驱动的.

Marijn G J Ford1, Ian G Mills, Brian J Peter

  • 1MRC Laboratory of Molecular Biology, Cambridge, UK.

Nature
|September 28, 2002
PubMed
概括

埃普辛1蛋白直接诱导膜曲在克拉斯林介导的内细胞因子通过插入一个α螺旋到脂质二层,促进囊泡的形成. 这种大脑丰富的蛋白质对于细胞膜动态至关重要.

科学领域:

  • 细胞生物学 细胞生物学
  • 生物化学 生物化学
  • 分子生物学分子生物学

背景情况:

  • 克拉特林介导的内细胞分裂 (CME) 对于细胞过程至关重要.
  • CME需要蛋白质层组装和膜变形.
  • 正在调查CME中特定蛋白质 (如epsin 1) 的作用.

研究的目的:

  • 调查CME中大脑丰富蛋白质epsin 1的功能.
  • 阐明epsin 1影响膜曲率的机制.
  • 确定epsin 1与酸丁酸-4,5-双酸盐 (PtdIns(4,5) P(2) 的相互作用在膜曲中的作用.

主要方法:

  • 研究了epsin 1与PtdIns的相互作用{4,5) P{2).
  • 分析了epsin 1和PtdIns(4,5) P(2) 对膜曲率的影响.
  • 利用位点定向的突变发生来探测epsin 1的两位传动性α-helix的功能.
  • 在脂质单层上进行了实验,以评估epsin 1诱导阴道的能力.

主要成果:

  • 素1与PtdIns{4,5) P{2) 结合,直接改变了膜曲率.
  • 在epsin 1中形成一个两形阿尔法螺旋链与PtdIns(4,5) P(2) 结合.

更多相关视频

Visualizing Clathrin-mediated Endocytosis of G Protein-coupled Receptors at Single-event Resolution via TIRF Microscopy
12:40

Visualizing Clathrin-mediated Endocytosis of G Protein-coupled Receptors at Single-event Resolution via TIRF Microscopy

Published on: October 20, 2014

Pulling Membrane Nanotubes from Giant Unilamellar Vesicles
06:26

Pulling Membrane Nanotubes from Giant Unilamellar Vesicles

Published on: December 7, 2017

相关实验视频

Last Updated: May 7, 2026

In vivo and in vitro Studies of Adaptor-clathrin Interaction
17:14

In vivo and in vitro Studies of Adaptor-clathrin Interaction

Published on: January 27, 2011

Visualizing Clathrin-mediated Endocytosis of G Protein-coupled Receptors at Single-event Resolution via TIRF Microscopy
12:40

Visualizing Clathrin-mediated Endocytosis of G Protein-coupled Receptors at Single-event Resolution via TIRF Microscopy

Published on: October 20, 2014

Pulling Membrane Nanotubes from Giant Unilamellar Vesicles
06:26

Pulling Membrane Nanotubes from Giant Unilamellar Vesicles

Published on: December 7, 2017

  • 这种螺旋体中疏水性残留物的突变阻止了膜曲率的诱导.
  • 单独的Epsin 1可以在脂质单层上促进克拉斯林涂层的侵染.
  • 结论:

    • 埃普辛1使用诱导的两形阿尔法螺旋在CME期间直接曲膜.
    • 这种螺旋可能会插入脂质双层,促进囊泡的形成.
    • 素1是克拉林介导的内分细胞分裂中膜曲率的关键媒介.