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相关概念视频

Protein Dynamics in Living Cells01:19

Protein Dynamics in Living Cells

2.1K
Different fluorescence-based techniques are used to study the protein dynamics in living cells. These techniques include FRAP, FRET, and PET.
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...
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Protein Diffusion in the Membrane01:24

Protein Diffusion in the Membrane

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Proteins show rotational as well as lateral diffusion across the membrane. The lateral diffusion of proteins was confirmed through the cell fusion experiment where mouse and human cells were fused, resulting in hybrid cells. When the human and mouse cells fused, the specific membrane proteins on human and mouse cells were marked with the red and green-fluorescent markers, respectively. Initially, the red and green fluorescence was located on the respective hemisphere of the cell. As time...
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相关实验视频

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High-resolution Spatiotemporal Analysis of Receptor Dynamics by Single-molecule Fluorescence Microscopy
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High-resolution Spatiotemporal Analysis of Receptor Dynamics by Single-molecule Fluorescence Microscopy

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另一种方法可视化细胞膜中的受体动态.

Ravelli Cosetta1,2, Corsini Michela1,2, Ventura Anna1

  • 1Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.

PloS one
|June 11, 2024
PubMed
概括

这项研究引入了一种更快的方法来观察所有膜受体及其随时间的位置. 该技术使用对活细胞的结构化照明显微镜,为FRAP和SPT提供了一种节省时间的替代方案.

科学领域:

  • 细胞生物学 细胞生物学
  • 生物物理学的生物物理.
  • 显微镜的使用方法

背景情况:

  • 膜受体动态对于细胞功能至关重要.
  • 像FRAP和SPT这样的当前方法耗时,并分析有限的细胞区域或受体数量.

研究的目的:

  • 开发一种节省时间的协议,可可视化整个膜受体池及其定位.
  • 为现有的资源密集型显微镜技术提供替代方案.

主要方法:

  • 采用光显微镜与结构化照明分割用于活细胞成像.
  • 能够可视化整个受体池及其时空定位.

主要成果:

  • 提供了一种实时观察整个膜受体群体的方法.
  • 显著减少图像采集和分析的时间 (两天).

结论:

  • 拟议的协议提供了一种有效的方式来研究膜受体动力学和多蛋白质复合体.
  • 适用于描述活细胞中对激活剂或抑制剂的受体反应.

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Imaging pHluorin-tagged Receptor Insertion to the Plasma Membrane in Primary Cultured Mouse Neurons
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