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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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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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Overview of Secretory Vesicles01:33

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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...
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Chemical Synapses01:26

Chemical Synapses

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Chemical synapses are specialized sites between two neurons or between a neuron and a non-neuronal cell like a muscle, glandular or sensory cell.
Because chemical synapses depend on the release of neurotransmitter molecules from synaptic vesicles to pass on their signal, there is an approximately one millisecond delay between when the axon potential reaches the presynaptic terminal and when the neurotransmitter leads to opening of postsynaptic ion channels. Additionally, this signaling is...
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Pinching-off of Coated Vesicles01:32

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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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Regulation of Nuclear Protein Sorting01:45

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Nuclear protein sorting regulates nucleus composition and gene expression, crucial for determining the fate of a eukaryotic cell. Hence, the entry and exit of molecules across the nuclear envelope is a tightly controlled process. Nuclear protein sorting can be inhibited by one of the following ways: 1) masking cargo signal sequences, 2) modifying the nuclear receptor's affinity for cargo, 3) controlling the nuclear pore size, 4) retaining the cargo during its transit to the cytosol or the...
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相关实验视频

Updated: Jul 12, 2025

An Optical Assay for Synaptic Vesicle Recycling in Cultured Neurons Overexpressing Presynaptic Proteins
09:33

An Optical Assay for Synaptic Vesicle Recycling in Cultured Neurons Overexpressing Presynaptic Proteins

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突触凝结控制突触囊泡封存和动态的突触凝结.

Christian Hoffmann1, Jakob Rentsch2, Taka A Tsunoyama3

  • 1Laboratory of Molecular Neuroscience, German Center for Neurodegenerative Diseases (DZNE), 10117, Berlin, Germany.

Nature communications
|October 23, 2023
PubMed
概括
此摘要是机器生成的。

突触囊泡 (SVs) 由于由SVs和突触素1形成的类似液体的凝聚物,在突触处受到限制和运动. 这种相互作用确保了神经元传播的可靠的SV行为.

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Measuring Synaptic Vesicle Endocytosis in Cultured Hippocampal Neurons
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An Optical Assay for Synaptic Vesicle Recycling in Cultured Neurons Overexpressing Presynaptic Proteins
09:33

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Measuring Synaptic Vesicle Endocytosis in Cultured Hippocampal Neurons
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Presynapse Formation Assay Using Presynapse Organizer Beads and “Neuron Ball” Culture
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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:

  • 神经传输取决于从突触囊泡 (SVs) 中调节的神经递质的释放.
  • 在突触中,SV的限制和移动性对于快速释放神经递质至关重要,但人们对其了解甚少.
  • Synapsin 1 是一种高度丰富的突触蛋白,参与SV调节.

研究的目的:

  • 阐明突触囊泡封闭和运动背后的机制.
  • 调查突触素1在组织突触囊泡中的作用.

主要方法:

  • 在复制的SV系统和活神经元中超快单分子追踪 (SMT).
  • 双色SMT和超分辨率成像在活的轴突中.
  • 使用突触三重敲击动物进行的实验.

主要成果:

  • 突触囊泡和突触素1形成类似液体的凝结物.
  • 突触素1减缓了它在这些凝聚物中的运动,这表明包装增加.
  • 交素1驱动了瘤中的SV积累,并恢复了本源的SV运动模式,即使是短片.

结论:

  • 突触素1的凝结足以确保突触囊泡的限制和运动性.
  • 这一过程使得SVs在活体突触中形成中大尺度域.
  • 突触素1在组织SVs中起着至关重要的作用,以实现高效的神经元信号传递.