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相关概念视频

Cryo-electron Microscopy01:28

Cryo-electron Microscopy

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Conventional electron microscopy (EM) involves dehydration, fixation, and staining of biological samples, which distorts the native state of biological molecules and results in several artifacts. Also, the high-energy electron beam damages the sample and makes it difficult to obtain high-resolution images. These issues can be addressed using cryo-EM, which uses frozen samples and gentler electron beams. The technique was developed by Jacques Dubochet, Joachim Frank, and Richard Henderson, for...
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Overview of Electron Microscopy01:25

Overview of Electron Microscopy

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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.
8.3K
Preparation of Samples for Electron Microscopy01:20

Preparation of Samples for Electron Microscopy

5.3K
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...
5.3K
Transmission Electron Microscopy01:15

Transmission Electron Microscopy

5.2K
In 1931, physicist Ernst Ruska—building on the idea that magnetic fields can direct an electron beam just as lenses can direct a beam of light in an optical microscope—developed the first prototype of the electron microscope. This development led to the development of the field of electron microscopy. In the transmission electron microscope (TEM), electrons are produced by a hot tungsten element and accelerated by a potential difference in an electron gun, which gives them up to 400...
5.2K
Scanning Electron Microscopy01:07

Scanning Electron Microscopy

4.0K
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...
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Electron Microscope Tomography and Single-particle Reconstruction01:07

Electron Microscope Tomography and Single-particle Reconstruction

2.3K
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...
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相关实验视频

Updated: May 7, 2025

Cell Culture on Silicon Nitride Membranes and Cryopreparation for Synchrotron X-ray Fluorescence Nano-analysis
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具有基本灵敏度的冷电子显微镜.

Hannah Ochner1, Tanmay A M Bharat1

  • 1Structural Studies Division, MRC Laboratory of Molecular Biology, Cambridge CB2 0QH, UK.

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此摘要是机器生成的。

研究人员开发了一种新技术,将电子能量损失光谱学和冷电子显微镜结合起来,用于对宏分子的元素映射. 这种方法提供了对分子组成的空间解析见解.

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Manual Blot-and-Plunge Freezing of Biological Specimens for Single-Particle Cryogenic Electron Microscopy
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Optimized Negative Staining: a High-throughput Protocol for Examining Small and Asymmetric Protein Structure by Electron Microscopy
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Manual Blot-and-Plunge Freezing of Biological Specimens for Single-Particle Cryogenic Electron Microscopy
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科学领域:

  • 结构生物学是结构生物学.
  • 生物物理学的生物物理.
  • 分析化学是一种分析化学.

背景情况:

  • 了解宏分子的元素组成对于阐明它们的结构和功能至关重要.
  • 现有的技术往往缺乏详细分析所需的空间分辨率或元素特异性.

研究的目的:

  • 开发和演示一种新的相关成像方法,用于高分辨率的生物宏分子元素映射.
  • 为了使分子分布在复杂的分子组合中的研究.

主要方法:

  • 相关成像技术将电子能量损失光谱学 (EELS) 与单粒子冷电子显微镜 (cryo-EM) 结合起来.
  • 空间分辨率EELS获取在冷-EM电网上以确定元素组成.
  • 将光谱数据与来自冷EM的结构信息进行整合.

主要成果:

  • 成功地实现了宏分子的空间分辨率元素映射.
  • 证明了在宏分子结构中识别和定位特定元素的能力.
  • 综合方法为元素分布提供了前所未有的细节.

结论:

  • 集成的EELS和冷EM技术为宏分子的结构和组成分析提供了一个强大的新工具.
  • 这种方法为研究特定元素在纳米级生物过程中的作用开辟了新的途径.
  • 未来的应用包括分析金属蛋白,核酸和其他含有元素的生物分子.