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相关概念视频

Pinching-off of Coated Vesicles01:32

Pinching-off of Coated Vesicles

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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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Clathrin Coated Vesicles01:12

Clathrin Coated Vesicles

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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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COP Coated Vesicles00:59

COP Coated Vesicles

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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...
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Receptor Downregulation in MVBs01:15

Receptor Downregulation in MVBs

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Multivesicular bodies (MVBs) are mature endosomes that sort ubiquitinated proteins and then fuse with lysosomes to degrade the sorted proteins. Epidermal growth factor (EGF) and its receptor (EGFR) form a complex that can be internalized through endocytosis, sorted into an MVB, and later degraded.
The EGFR can initiate signaling pathways that  lead to cell proliferation, migration, and differentiation. Overexpression of EGFR  stimulates cells to proliferate. Excessive  EGFR...
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Intralumenal Vesicles and Multivesicular Bodies01:38

Intralumenal Vesicles and Multivesicular Bodies

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Intraluminal vesicles (ILVs) are small vesicles 50-80 nm in diameter formed during the maturation of early endosomes. A specialized endosome containing numerous ILVs is called a multivesicular body (MVB). ILVs contain internalized molecules such as antigens, nucleic acids, proteins, and metabolites. Some of these molecules are released from the MVBs inside exosomes and are transported to other cells. Other MVBs contain molecules that are retained in the ILVs and are later degraded within the...
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Vesicular Tubular Clusters01:45

Vesicular Tubular Clusters

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After budding out from the ER membrane, some COPII vesicles lose their coat and fuse with one another to form larger vesicles and interconnected tubules called vesicular tubular clusters or VTCs. These clusters constitute a compartment at the ER-Golgi interface known as ERGIC (Endoplasmic Reticulum Golgi Intermediate Compartment). The ERGIC is a mobile membrane-bound cargo transport system that sorts proteins secreted from ER and delivers them to the Golgi.
With the help of motor proteins such...
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相关实验视频

Updated: May 27, 2025

In Vesiculo Synthesis of Peptide Membrane Precursors for Autonomous Vesicle Growth
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In Vesiculo Synthesis of Peptide Membrane Precursors for Autonomous Vesicle Growth

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双响应性双阻塞共聚囊的触发反转

Casey A Morrison1, Ethan P Chan1, Timothy J Deming1,2

  • 1Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095, United States.

Journal of the American Chemical Society
|February 20, 2025
PubMed
概括

研究人员制造出一种自组装成囊泡的新型双阻塞共聚. 这些合成组件对刺激做出反应, 破坏或逆转成新的结构, 显示生物医学应用的潜力.

科学领域:

  • 聚合物化学
  • 材料科学
  • 生物材料

背景情况:

  • 两块共聚物对于自组装成纳米结构至关重要.
  • 开发模仿生物功能的合成材料是材料科学中的一个关键挑战.

研究的目的:

  • 合成和表征新型的两性双块共聚,聚甲硫化物) - - 聚甲 (MA).
  • 研究这些共聚的自我组装行为.
  • 探索这些囊泡的刺激反应特性,

主要方法:

  • 合成两性多甲硫化) -b多甲氨酸) 双块共.
  • 使用显微镜和动态光散射对自组装结构的描述.
  • 在生理条件下用谷氨和硫糖酸进行化.

主要成果:

  • 成功合成了MA共聚,可以自组成亚微米单囊.
  • 由于独特的疏水性质,在广泛的成分中发生了囊泡形成.
  • 囊泡表现出对刺激的反应行为,经过谷氨的干扰和硫糖酸的逆转.

结论:

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Phase Behavior of Charged Vesicles Under Symmetric and Asymmetric Solution Conditions Monitored with Fluorescence Microscopy
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Phase Behavior of Charged Vesicles Under Symmetric and Asymmetric Solution Conditions Monitored with Fluorescence Microscopy

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Membrane Remodeling of Giant Vesicles in Response to Localized Calcium Ion Gradients

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Phase Behavior of Charged Vesicles Under Symmetric and Asymmetric Solution Conditions Monitored with Fluorescence Microscopy
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Phase Behavior of Charged Vesicles Under Symmetric and Asymmetric Solution Conditions Monitored with Fluorescence Microscopy

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  • 在水性介质中,MA共聚形成稳定,响应的囊泡.
  • 在生理条件下使用生物相关刺激来破坏或逆转囊泡的能力是前所未有的.
  • 这些发现为开发用于生物和医学应用的先进功能合成组件提供了新的途径.