通过多维单分子和超分辨率显微镜探测细胞膜中的纳米扩散异质性
Rui Yan1,2, Kun Chen1,2, Ke Xu1,2
1Department of Chemistry, University of California, Berkeley, California 94720, United States.
Journal of the American Chemical Society
|October 21, 2020
概括
活细胞膜扩散会随着脂肪的增加而减缓. 研究人员绘制了膜地形和扩散性,发现蛋白质聚集,而不是脂质顺序,导致特定接触点的减速.
科学领域:
- 生物物理
- 细胞生物学
- 膜动力学
背景情况:
- 生物膜扩散对于细胞功能至关重要.
- 了解纳米扩散异质性是细胞生物学的关键.
研究的目的:
- 在活哺乳动物细胞中同时绘制纳米级膜拓,扩散性和脂质包装顺序.
- 研究细胞膜中扩散异质性的起源.
主要方法:
- 开发了一种新型的脂性光启动探针,用于持续的单分子成像.
- 结合单分子成像与超分辨率显微镜进行纳米尺度映射.
- 使用光谱分辨率的单分子成像来区分扩散原因.
主要成果:
- 在不同膜区域 (ER,血膜,纳米域) 中,减少了膜扩散性和增加了脂质包装顺序之间的相关性.
- 在内细胞膜接触部位发现扩散性降低.
- 证明接触点的局部扩散减缓是由于蛋白质拥挤而不是脂质包装的改变.
结论:
- 集成的多维单分子方法成功地绘制了纳米级膜特性.
- 基于其起源的纳米扩散异质 (脂质包装与蛋白质拥挤).
- 提供了对特定细胞位置膜动态调节的新见解.
更多相关视频
相关概念视频
Super-resolution Fluorescence Microscopy
12.0K
Super-resolution fluorescence microscopy (SRFM) provides a better resolution than conventional fluorescence microscopy by reducing the point spread function (PSF). PSF is the light intensity distribution from a point that causes it to appear blurred. Due to PSF, each fluorescing point appears bigger than its actual size, and it is the PSF interference of nearby fluorophores that causes the blurred image. Various approaches to achieving higher resolution through SRFM have recently been...
12.0K
Protein Diffusion in the Membrane
5.2K
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...
5.2K
Protein Dynamics in Living Cells
2.5K
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...
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...
2.5K


