扫描离子导电显微镜用于研究活细胞表面β-粉样聚合物的形成
Vasilii S Kolmogorov1,2, Alexander S Erofeev1, Evgeny P Barykin3
1National University of Science and Technology "MISIS", 119049 Moscow, Russian Federation.
Analytical chemistry
|October 19, 2023
概括
细胞表面的β-粉样蛋白 (Aβ) 聚合会通过改变细胞机制引起神经毒性. 这项研究将Aβ诱导的氧化应激与细胞的变化联系起来年轻年轻.
科学领域:
- 神经科学是一个神经科学.
- 生物物理学的生物物理.
- 细胞生物学 细胞生物学
背景情况:
- 在神经元表面的β-粉样蛋白 (Aβ) 聚合与神经退行性疾病有关.
- 亚β聚合通过流入,亡和减少膜潜力来破坏细胞功能.
- 细胞骨的变化,特别是动蛋白和微管,改变细胞的机械性质.
研究的目的:
- 研究细胞膜上的Aβ聚合物形成与局部细胞机械性质的变化之间的精确联系.
- 探索反应性氧物种 (ROS) 在调解Aβ诱导的细胞力学变化的作用.
主要方法:
- 相对扫描离子导电显微镜 (SICM) 用于细胞拓,模量映射和Aβ聚合物的共聚焦成像.
- 使用纳米电极测量细胞内活性氧物种 (ROS) 水平.
主要成果:
- SICM成功地绘制了Aβ聚合物形成的地图,并将其与细胞Young模量变化相关联.
- 观察到Aβ诱导的氧化应激和细胞内ROS水平的增加.
- 证明了ROS水平与细胞模量变化之间的直接联系.
结论:
- 活细胞表面的Aβ聚合显著影响细胞力学.
- 反应性氧物种在调解由Aβ引起的机械变化方面发挥着至关重要的作用.
- SICM是研究Aβ聚合物的细胞毒性机制的一个有价值的工具.
更多相关视频
09:31Visualization of Amyloid β Deposits in the Human Brain with Matrix-assisted Laser Desorption/Ionization Imaging Mass Spectrometry
Published on: March 7, 2019
10.7K
08:25Detecting Amyloid-β Accumulation via Immunofluorescent Staining in a Mouse Model of Alzheimer's Disease
Published on: April 19, 2021
3.3K
相关概念视频
Overview of Electron Microscopy
The wavelengths of visible light ultimately limit the maximum theoretical resolution of images created by light microscopes. Most light microscopes can only magnify 1000X, and a few can magnify up to 1500X. Electrons, like electromagnetic radiation, can behave like waves, but with wavelengths of 0.005 nm, they produce significantly greater resolution up to 0.05 nm as compared to 500 nm for visible light. An electron microscope (EM) can create a sharp image that is magnified up to 2,000,000X.
Scanning Electron Microscopy
A scanning electron microscope (SEM) is used to study the surface features of a sample by using an electron beam that scans the sample surface in a two-dimensional manner. Typically, areas between ~1 centimeter to 5 micrometers in width can be imaged. SEM can be used to image bacteria, viruses, tissues as well as larger samples like insects. Conventional SEM gives a magnification ranging from 20X to 30,000X and spatial resolution of 50 to 100 nanometers.
Fundamental Principles
Accelerated...
Fundamental Principles
Accelerated...
Preparation of Samples for Electron Microscopy
To be visualized by an electron microscope, either transmission or scanning, biological samples need to be fixed (stabilized) so the electron beam does not destroy them and dried thoroughly (desiccated/dehydrated) so the vacuum does not affect them. Fixation needs to be done as quickly as possible because the sample properties will start changing as soon as it is removed from its natural environment. For example, in a tissue sample, the oxygen levels begin decreasing, causing an altered...
Electron Microscope Tomography and Single-particle Reconstruction
Transmission electron microscopy (TEM) can be used to determine the 3D structure of biological samples with the help of techniques such as electron microscope tomography and single-particle reconstruction. While single-particle reconstruction can examine macromolecules and macromolecular complexes in vitro conditions only, tomography permits the study of cell components or small cells in vivo.
Electron Tomography
Electron tomography can be performed either in TEM or STEM (scanning transmission...
Electron Tomography
Electron tomography can be performed either in TEM or STEM (scanning transmission...
Overview of Microscopy Techniques
The early pioneers of microscopy opened a window into the invisible world of microorganisms. In 1830, Joseph Jackson Lister created an essentially modern light microscope. The 20th century saw the development of microscopes that leveraged nonvisible light, such as fluorescence microscopy that uses an ultraviolet light source and electron microscopy that uses short-wavelength electron beams. These advances significantly improved magnification, image resolution, and contrast. By comparison, the...
