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関連する概念動画

Fusion of Secretory Vesicles with the Plasma Membrane01:26

Fusion of Secretory Vesicles with the Plasma Membrane

16.0K
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...
16.0K
Pinching-off of Coated Vesicles01:32

Pinching-off of Coated Vesicles

3.2K
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...
3.2K
SNAREs and Membrane Fusion01:43

SNAREs and Membrane Fusion

10.5K
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...
10.5K
Vesicular Tubular Clusters01:45

Vesicular Tubular Clusters

2.5K
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...
2.5K
Clathrin Coated Vesicles01:12

Clathrin Coated Vesicles

8.2K
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...
8.2K
Rab Cascades01:25

Rab Cascades

2.9K
Rab GTPases act in a regulated cascade during membrane fusion, helping the lipid bilayers mix. The Rab family of proteins are active when bound to GTP, and inactive when bound to GDP. Hence, they act as guanine nucleotide-dependent molecular switches. Rab-GTP recognizes and binds to long or short-range tethering proteins to capture the target vesicle. These tethers coordinate with SNAREs on the vesicle and the target membrane to assemble the trans SNARE complex that locks the mixing bilayers.
2.9K

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Synaptophysin accelerates synaptic vesicle fusion by expanding the membrane upon neurotransmitter loading.

Science advances·2025
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Isolating Synaptic Vesicles from Neurospheres for Proteomics.

Methods in molecular biology (Clifton, N.J.)·2024
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Intermediate steps in the formation of neuronal SNARE complexes.

The Journal of biological chemistry·2024
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Rab GTPases and phosphoinositides fine-tune SNAREs dependent targeting specificity of intracellular vesicle traffic.

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Vesicle condensation induced by synapsin: condensate size, geometry, and vesicle shape deformations.

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関連する実験動画

Updated: May 5, 2026

Analysis of SNARE-mediated Membrane Fusion Using an Enzymatic Cell Fusion Assay
09:19

Analysis of SNARE-mediated Membrane Fusion Using an Enzymatic Cell Fusion Assay

Published on: October 19, 2012

13.1K

テザリング・コンプレックスは,SNAREを募集し,ベジクルを捕まえる.

Hans Dieter Schmitt1, Reinhard Jahn

  • 1Department of Neurobiology, Max-Planck-Institute for Biophysical Chemistry, 37077 Göttingen, Germany.

Cell
|December 17, 2009
PubMed
まとめ

イーストのDSL1複合体は,タンパク質・テンダーとして働き,ベジクルをエンドプラズマ網膜 (ER) に接続します. ER SNAREのタンパク質と結合し,回路を使って膀を捕獲し,膜の隙間を埋める.

科学分野:

  • 細胞生物学 細胞生物学
  • メンブラン密輸 膜密輸
  • タンパク質とタンパク質の相互作用

背景:

  • タンパク質の結合は,膜の隙間を埋めるために極めて重要です.
  • 膀-ERの相互作用を理解することは,細胞機能の鍵です.

研究 の 目的:

  • イーストのDSL1複合体が結晶をエンドプラズマ網膜 (ER) に結合させるメカニズムを調査する.

主な方法:

  • タンパク質結合を研究するための生化学分析.
  • Dsl1複合体の形状を理解するための構造分析.

主要な成果:

  • Dsl1複合体は,ER SNAREタンパク質を基底に結合する.
  • ER膜から20nmまで広がるループ領域は,小胞を捕まえます.
  • この相互作用によって,膀がERに効果的に結合します.

結論:

  • Dsl1複合体は,膀とERの間の特定の結合として機能します.
  • その構造は,膀-ER接続の捕捉と安定化を容易にする.

さらに関連する動画

SNARE-mediated Fusion of Single Proteoliposomes with Tethered Supported Bilayers in a Microfluidic Flow Cell Monitored by Polarized TIRF Microscopy
10:58

SNARE-mediated Fusion of Single Proteoliposomes with Tethered Supported Bilayers in a Microfluidic Flow Cell Monitored by Polarized TIRF Microscopy

Published on: August 24, 2016

10.6K
Visualizing Intracellular SNARE Trafficking by Fluorescence Lifetime Imaging Microscopy
08:55

Visualizing Intracellular SNARE Trafficking by Fluorescence Lifetime Imaging Microscopy

Published on: December 29, 2017

11.0K

関連する実験動画

Last Updated: May 5, 2026

Analysis of SNARE-mediated Membrane Fusion Using an Enzymatic Cell Fusion Assay
09:19

Analysis of SNARE-mediated Membrane Fusion Using an Enzymatic Cell Fusion Assay

Published on: October 19, 2012

13.1K
SNARE-mediated Fusion of Single Proteoliposomes with Tethered Supported Bilayers in a Microfluidic Flow Cell Monitored by Polarized TIRF Microscopy
10:58

SNARE-mediated Fusion of Single Proteoliposomes with Tethered Supported Bilayers in a Microfluidic Flow Cell Monitored by Polarized TIRF Microscopy

Published on: August 24, 2016

10.6K
Visualizing Intracellular SNARE Trafficking by Fluorescence Lifetime Imaging Microscopy
08:55

Visualizing Intracellular SNARE Trafficking by Fluorescence Lifetime Imaging Microscopy

Published on: December 29, 2017

11.0K