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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

19.2K
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...
19.2K
Pore Size Distribution01:23

Pore Size Distribution

538
In concrete, the pore size distribution significantly influences the material's properties. Capillary pores, markedly larger than gel pores, form a vast network within partially hydrated cement paste, reducing the concrete's strength and increasing its permeability. This heightened permeability leads to a greater risk of damage from environmental factors like freeze-thaw cycles and chemical attacks, with the extent of vulnerability also being tied to the water-to-cement ratio.
Adequate...
538
SNAREs and Membrane Fusion01:43

SNAREs and Membrane Fusion

13.2K
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...
13.2K
Enlargement of the Plasma Membrane01:22

Enlargement of the Plasma Membrane

2.6K
Cell division and enlargement are processes that require precise control. The control ensures that cell division cannot proceed unless the cell has grown to a specific size. A spherical, dividing cell requires an approximately 1.6X increase in its surface area to double its volume. The secretory pathway also has a significant role in cell membrane enlargement. Secretory vesicles that bud off from the Golgi apparatus and later fuse with the plasma membrane during exocytosis are a major source of...
2.6K
Porin Insertion in the Outer Mitochondrial Membrane01:12

Porin Insertion in the Outer Mitochondrial Membrane

5.1K
Porins are beta-barrel proteins translocated to the mitochondrial outer membrane through the TOM complex into the intermembrane space. Porin precursors bind TIM chaperones within the intermembrane space and are guided to the Sorting and Assembly Machinery complex or SAM complex on the outer mitochondrial membrane.
Three models describe the assembly of porins by the SAM complex and their insertion into the outer membrane. Model 1 suggests that porins are assembled outside the SAM channel as the...
5.1K
Structure of Porins01:21

Structure of Porins

4.1K
Mitochondria, chloroplasts, and gram-negative bacteria have transmembrane, beta-barrel proteins called porins to mediate the free diffusion of ions and metabolites across the membrane. Mitochondrial porin precursors contain conserved amino acid sequences called beta signals at their C-terminal. Beta signals have a  motif of PoXGXXHyXHy (Po-Polar, X-Any amino acid, G-Glycine, Hy-LargeHydrophobic), which are crucial for precursor recognition to initiate precursor assembly. Beta-barrel...
4.1K

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相关实验视频

Updated: Mar 12, 2026

Confocal Microscopy to Measure Three Modes of Fusion Pore Dynamics in Adrenal Chromaffin Cells
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Confocal Microscopy to Measure Three Modes of Fusion Pore Dynamics in Adrenal Chromaffin Cells

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一个融合孔有多大?

Meyer B Jackson1

  • 1Department of Neuroscience, University of Wisconsin - Madison.

Biophysical journal
|March 11, 2026
PubMed
概括

这项研究澄清了聚孔大小测量在外细胞突变. 调和不同的结果,它表明基于流量的方法可能低估了初始的融合孔径,突出了生物相关的变化.

科学领域:

  • 细胞生物学 细胞生物学
  • 生物物理学的生物物理.

背景情况:

  • 融合孔对于理解外细胞和膜融合机制至关重要.
  • 估计聚变孔径具有挑战性,目前的方法产生了截然不同的结果.

研究的目的:

  • 批判性地评估确定融合孔径的方法.
  • 为了协调融合孔径大小估计的差异,并确定一个基本的结构.

主要方法:

  • 审查和评估用于估计融合孔径的结构和生理技术.
  • 分析流量测量模型,特别是圆柱形孔模型.

主要成果:

  • 基于流量的直径估计可能会系统地低估实际的孔径大小.
  • 专注于最初的融合孔状况,可以发现一个独特的结构.
  • 考虑到建模的局限性,可以缩小初始聚变孔的大小范围.

结论:

  • 通过对方法的批判性评估,可以减少聚变孔尺寸估计的差异.
  • 最初的融合孔径大小可能会表现出生物学上显著的变化.

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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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Fine-tuning the Size and Minimizing the Noise of Solid-state Nanopores
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