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相关概念视频

SNAREs and Membrane Fusion01:43

SNAREs and Membrane Fusion

10.8K
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...
10.8K
Fusion of Secretory Vesicles with the Plasma Membrane01:26

Fusion of Secretory Vesicles with the Plasma Membrane

10.9K
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...
10.9K
Overview of Secretory Vesicles01:33

Overview of Secretory Vesicles

8.4K
Secretory vesicles, also known as dense core vesicles (DCVs), are membrane-bound vesicles that transport secretory proteins, such as hormones or neurotransmitters. Regulated secretory vesicles transport proteins from the trans-Golgi network to the exterior of the cell. Proteins present in regulated secretory vesicles are required to be rapidly exocytosed in large amounts upon a specific stimulus.
Various proteins regulate the aggregation of molecules inside the secretory vesicles. Chromogranins...
8.4K
Clathrin Coated Vesicles01:12

Clathrin Coated Vesicles

6.8K
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...
6.8K
Pinching-off of Coated Vesicles01:32

Pinching-off of Coated Vesicles

3.1K
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...
3.1K
The Early Endosome: Endocytosis of Transferrin01:28

The Early Endosome: Endocytosis of Transferrin

3.2K
Essential proteins such as insulin or low-density lipoprotein (LDL) and micronutrients such as iron enter a eukaryotic cell through receptor-mediated endocytosis. Subsequently, the early endosomes fuse with the vesicles containing such receptor-ligand complexes and play a vital role in sorting the incoming ligands and receptors. While the ligands are either degraded inside the vesicle or released into the cytosol, their receptors are returned to the plasma membrane for further rounds of...
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相关实验视频

Updated: Jun 4, 2025

Expression, Purification, and Liposome Binding of Budding Yeast SNX-BAR Heterodimers
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Expression, Purification, and Liposome Binding of Budding Yeast SNX-BAR Heterodimers

Published on: December 6, 2019

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内体组分类蛋白SNX4限制了突触囊泡的对接和释放.

Josse Poppinga1, Nolan J Barrett1, L Niels Cornelisse1,2

  • 1Department of Functional Genomics, Center for Neurogenomics and Cognitive Research (CNCR), VU University, Amsterdam, Netherlands.

eLife
|December 19, 2024
PubMed
概括

排序nexin 4 (SNX4) 在神经元中组织膜循环. 通过增加活性区域的突触囊泡密度,SNX4 枯竭增强了神经传递,这表明SNX4 对囊泡释放有负面调节.

关键词:
细胞生物学 细胞生物学海马神经元的神经元这里是鼠标鼠标鼠标鼠标鼠标鼠标.神经科学 神经科学神经传递传递是神经的传递.塑性的可塑性 塑性循环回收内分泌体的内分泌体囊泡的招募 囊泡的招募

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Measuring Synaptic Vesicle Endocytosis in Cultured Hippocampal Neurons
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Measuring Synaptic Vesicle Endocytosis in Cultured Hippocampal Neurons

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Visualizing Intracellular SNARE Trafficking by Fluorescence Lifetime Imaging Microscopy
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Visualizing Intracellular SNARE Trafficking by Fluorescence Lifetime Imaging Microscopy

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相关实验视频

Last Updated: Jun 4, 2025

Expression, Purification, and Liposome Binding of Budding Yeast SNX-BAR Heterodimers
10:28

Expression, Purification, and Liposome Binding of Budding Yeast SNX-BAR Heterodimers

Published on: December 6, 2019

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Measuring Synaptic Vesicle Endocytosis in Cultured Hippocampal Neurons
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Measuring Synaptic Vesicle Endocytosis in Cultured Hippocampal Neurons

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Visualizing Intracellular SNARE Trafficking by Fluorescence Lifetime Imaging Microscopy
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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
  • 分子生物学分子生物学

背景情况:

  • 排序nexin 4 (SNX4) 对于膜循环至关重要,在神经元突触中发现.
  • 目前尚不清楚SNX4在突触功能和神经传递中的确切作用.

研究的目的:

  • 研究SNX4在调节突触传输和结构中的功能.
  • 确定SNX4如何影响神经递质释放和突触中的囊泡动力学.

主要方法:

  • 生成一个有条件的SNX4淘汰 (cKO) 鼠标模型.
  • 电生理学记录以评估神经传递和突触功能.
  • 通过电子显微镜分析突触超结构和突触囊泡定位.

主要成果:

  • 在高频刺激期间,SNX4 cKO突触表现出增强的神经传递,基础神经传递正常.
  • 突触超结构分析显示,在活跃区域的突触囊泡数量增加,活跃区域的长度减少.
  • SNX4的耗尽并没有改变整体囊泡数量,循环,或像VAMP2这样的关键蛋白质的水平.

结论:

  • SNX4作为突触囊泡对接和神经递质释放的负调节者.
  • 在活性区域中,SNX4在调节突触囊泡招募和密度方面发挥着重要作用.
  • 这些发现凸显了SNX4在突触可塑性和功能中的重要性.