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Videos de Conceptos Relacionados

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

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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...
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...
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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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A versatile nanobody platform for live and super-resolution imaging of synaptic vesicle dynamics and plasticity in rodent and human neurons.

Journal of nanobiotechnology·2026
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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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Rab GTPases and phosphoinositides fine-tune SNAREs dependent targeting specificity of intracellular vesicle traffic.

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Video Experimental Relacionado

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

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Un complejo de atadura recluta SNAREs y agarra las vesículas.

Hans Dieter Schmitt1, Reinhard Jahn

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

Cell
|December 17, 2009
PubMed
Resumen

El complejo Dsl1 de la levadura actúa como un lazo de proteínas, conectando las vesículas con el retículo endoplasmático (ER). Se une a las proteínas ER SNARE y utiliza un bucle para capturar las vesículas, cerrando las brechas de la membrana.

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

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Visualizing Intracellular SNARE Trafficking by Fluorescence Lifetime Imaging Microscopy
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Last Updated: May 5, 2026

Analysis of SNARE-mediated Membrane Fusion Using an Enzymatic Cell Fusion Assay
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SNARE-mediated Fusion of Single Proteoliposomes with Tethered Supported Bilayers in a Microfluidic Flow Cell Monitored by Polarized TIRF Microscopy
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Visualizing Intracellular SNARE Trafficking by Fluorescence Lifetime Imaging Microscopy
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Área de la Ciencia:

  • Biología celular Biología celular.
  • El tráfico de membranas.
  • Las interacciones proteína-proteína.

Sus antecedentes:

  • Las ataduras de proteínas son cruciales para cerrar las brechas de la membrana.
  • Comprender las interacciones vesícula-ER es clave para la función celular.

Objetivo del estudio:

  • Investigar el mecanismo por el cual el complejo Dsl1 de la levadura ata las vesículas al retículo endoplasmático (ER).

Principales métodos:

  • Ensayos bioquímicos para estudiar la unión a las proteínas.
  • Análisis estructural para comprender la conformación del complejo Dsl1.

Principales resultados:

  • El complejo Dsl1 se une a las proteínas ER SNARE en su base.
  • Una región de bucle que se extiende 20 nm desde la membrana ER captura las vesículas.
  • Esta interacción efectivamente ata las vesículas a la ER.

Conclusiones:

  • El complejo Dsl1 funciona como un lazo específico entre las vesículas y el ER.
  • Su estructura facilita la captura y estabilización de las conexiones vesícula-ER.