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相关概念视频

Super-resolution Fluorescence Microscopy01:37

Super-resolution Fluorescence Microscopy

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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...
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Overview of Electron Microscopy01:25

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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.
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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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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...
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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.
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The cytoskeletal architecture can be studied using different microscopic and biochemical techniques. Electron microscopy was instrumental in discovering the cytoskeletal architecture around the 1960s, which allowed obtaining structural information at a high-resolution level. However, the sample preparation procedure often limits this ability in biological samples. Several protocols have been developed over the years to optimize sample preparation. In one of the protocols known as rotary...
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相关实验视频

Updated: May 24, 2025

Nano-fEM: Protein Localization Using Photo-activated Localization Microscopy and Electron Microscopy
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分子差异化编码显微镜在空间分辨率以下的细胞纳米环境中剖析密集的生物分子.

Siyue Fan1, Xinyin Li1, Huan Liu1

  • 1Institute of Analytical Chemistry and Instrument for Life Science, The Key Laboratory of Biomedical Information Engineering of Ministry of Education, School of Life Science and Technology, Xi'an Jiaotong University, Xianning West Road, Xi'an, Shaanxi, 710049, China.

Angewandte Chemie (International ed. in English)
|March 4, 2025
PubMed
概括

这项研究引入了一种新的显微镜方法,使用DNA条形码来计算细胞内的密集生物分子. 这种技术克服了分辨率的限制,揭示了对生物功能至关重要的纳米级组织.

关键词:
细胞成像 细胞成像标记DNA的标记是指DNA的标记.数字化量化数字化量化分子拥挤是分子拥挤.分子分化的分化.

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科学领域:

  • 细胞和分子生物学 细胞和分子生物学
  • 纳米技术纳米技术
  • 生物物理学的生物物理.

背景情况:

  • 细胞生物分子在纳米尺度上组织得很密集,控制着重要的生物过程.
  • 目前的显微镜技术很难解决这些密集的生物分子的精确空间分布和复制数.

研究的目的:

  • 开发一种用于数字化量化细胞纳米环境内的密集生物分子的新方法.
  • 克服传统显微镜对纳米生物分析的空间分辨率限制.

主要方法:

  • 开发了一种分子分化编码显微镜 (MDEM) 技术,使用正交联重复DNA标识符.
  • 采用静态多重反应来条码单个生物分子副本与独特的DNA序列.
  • 创建了一个算法,用于自动量化重叠和单个分子斑点的量化.

主要成果:

  • 成功地可视化和量化了RNAs的密集分布,DNA表观遗传修饰和细胞表面甘氨酸/甘氨酸RNAs.
  • 证明各种生物分子在拥挤的细胞纳米环境中表现出密集的组织.
  • 在细胞表面纳米环境中定位的U1 glycoRNA副本中,平均有17%的量化.

结论:

  • 开发的MDEM战略使生物分子在显微镜空间分辨率以下的数字定量可视化成为可能.
  • 这种方法为细胞纳米环境中密集的生物分子组织的功能影响提供了关键的见解.