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相关概念视频

Fusion of Secretory Vesicles with the Plasma Membrane01:26

Fusion of Secretory Vesicles with the Plasma Membrane

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Proteins and neurotransmitters in secretory vesicles can be released from a cell upon vesicle docking, priming, and fusion with the plasma membrane. Vesicles are docked and primed in preparation for the quick exocytosis of their contents in response to a stimulus. The fusion process is mainly carried out by a SNAP Receptor or SNARE complex, consisting of synaptobrevin, syntaxin-1, and SNAP-25.
In 1993, Jim Rothman proposed that the antiparallel pairing of vesicular and transmembrane SNAREs, or...
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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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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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SNAREs and Membrane Fusion01:43

SNAREs and Membrane Fusion

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Once a transport vesicle has recognized its target organelle, the vesicular membrane needs to fuse with the target membrane to unload the cargo. Transmembrane proteins called SNAREs present on organelle membranes and their vesicles, mediate vesicle fusion.
SNAREs exist in pairs that symmetrically interact and catalyze the fusion of the lipid bilayers in vesicle and target organelle. v-SNARE in the vesicle membrane are single polypeptide chains that bind to a complementary t-SNARE, composed of 2...
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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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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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相关实验视频

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Visualization of Endosome Dynamics in Living Nerve Terminals with Four-dimensional Fluorescence Imaging
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在神经终端中,小型和大型密集核心囊泡的电容级和融合孔.

Vitaly A Klyachko1, Meyer B Jackson

  • 1Department of Physiology and Biophysics Graduate Program, University of Wisconsin-Madison, 1300 University Avenue, Madison, Wisconsin 53706, USA.

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|July 5, 2002
PubMed
概括
此摘要是机器生成的。

研究人员测量了神经终端中的单胞容量级,揭示了大型密核囊泡 (LDCV) 和微囊泡的独特融合过程. 这项研究有助于我们更好地理解神经系统中的细胞外形成机制.

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科学领域:

  • 神经科学是一个神经科学.
  • 细胞生物学 细胞生物学
  • 生物物理学的生物物理.

背景情况:

  • 神经终端利用大密核囊泡 (LDCVs) 和小突触囊泡释放神经递质.
  • 使用电容记录研究小突触囊泡的外细胞形成一直是具有挑战性的.
  • 后垂体神经终端中的微囊泡类似于突触囊泡,但其内容不明.

研究的目的:

  • 为了研究后垂体神经末端的单囊囊容量步骤.
  • 描述微粒细胞和LDCVs的外细胞形成机制.
  • 为了比较LDCVs和microvesicles的融合中间体.

主要方法:

  • 在后垂体神经终端的高分辨率电容记录.
  • 检测对应于囊泡融合的单元容量步骤.
  • 在外细胞形成过程中分析聚变孔导电性.

主要成果:

  • 检测到两种不同的电容级尺寸,对应于微微圈和LDCV.
  • 这两种囊泡类型都通过Ca(2+) 依赖的外细胞结合.
  • 微管和LDCV很少表现出亲吻和逃跑的外细胞,具有不同的融合孔尺寸 (19 pS对于微管和LDCV更大).

结论:

  • LDCVs和microvesicles在外细胞形成过程中使用结构上不同的融合中间体.
  • 容量测量提供了对不同类型囊泡的独特外细胞路径的洞察.
  • 这项研究阐明了神经末端囊泡融合背后的生物物理机制.