Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Scanning Electron Microscopy01:07

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...
Cryo-electron Microscopy01:28

Cryo-electron Microscopy

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

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...

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Unraveling Subcellular Ultrastructure with Cyclically Multiplexed Expansion Microscopy.

bioRxiv : the preprint server for biology·2026
Same author

Understanding microtubule dynamics: The synergy of technology, theory, and experiment.

The Journal of cell biology·2025
Same author

Mouse radial spoke 3 is a metabolic and regulatory hub in cilia.

Nature structural & molecular biology·2025
Same author

The cryo-EM structure of mouse radial spoke 3 reveals a unique metabolic and regulatory hub in cilia.

bioRxiv : the preprint server for biology·2025
Same author

High-Resolution Proteomics Unveils Salivary Gland Disruption and Saliva-Hemolymph Protein Exchange in <i>Plasmodium</i>-Infected Mosquitoes.

bioRxiv : the preprint server for biology·2025
Same author

Cryo-electron tomography of eel sperm flagella reveals a molecular "minimum system" for motile cilia.

Molecular biology of the cell·2024

相关实验视频

Updated: Jul 16, 2026

Fundamental Technical Elements of Freeze-fracture/Freeze-etch in Biological Electron Microscopy
11:17

Fundamental Technical Elements of Freeze-fracture/Freeze-etch in Biological Electron Microscopy

Published on: September 11, 2014

通过冷电子断层扫描揭示了轴膜的分子结构.

Daniela Nicastro1, Cindi Schwartz, Jason Pierson

  • 1Laboratory for 3D Electron Microscopy of Cells, Department of Molecular, Cellular, and Developmental Biology, CB 347, University of Colorado, Boulder, CO 80309-0347, USA. nicastro@colorado.edu

Science (New York, N.Y.)
|August 19, 2006
PubMed
概括

研究人员可视化了真核细胞鞭毛和眼的3D结构,揭示了运动蛋白质dynein如何产生力,以及其作用如何协调运动.

科学领域:

  • 细胞生物学 细胞生物学
  • 结构生物学 结构生物学
  • 生物物理学的生物物理.

背景情况:

  • 细胞的鞭毛和毛是复杂的细胞结构,对于运动性至关重要.
  • 核心结构,轴膜,由9+2的微管和250多种蛋白质组成,包括动力酶dynein.

研究的目的:

  • 用先进的成像技术阐明轴的三维结构.
  • 了解dynein为微管滑动产生力量的机制.
  • 确定参与协调运动蛋白活性的新型组件.

主要方法:

  • 低温电子断层扫描被用于从克拉米多马纳斯和海精子中快速结的轴膜的图像.
  • 使用先进的图像处理技术,专注于dynein运动酶.

主要成果:

  • 详细的3D轴膜结构模型被生成,突出突出dynein在力量产生中的作用.
  • 确定了两种新的dynein链接剂,表明了协调运动作用的机制.
  • 观察到双层微管体内的周期性密度,可能有助于结构稳定.

结论:

  • 这项研究为理解在乳毛和鞭毛中由dynein驱动的微管滑动提供了结构基础.

更多相关视频

Studying the Supramolecular Organization of Photosynthetic Membranes within Freeze-fractured Leaf Tissues by Cryo-scanning Electron Microscopy
13:52

Studying the Supramolecular Organization of Photosynthetic Membranes within Freeze-fractured Leaf Tissues by Cryo-scanning Electron Microscopy

Published on: June 23, 2016

Nanoscale Characterization of Liquid-Solid Interfaces by Coupling Cryo-Focused Ion Beam Milling with Scanning Electron Microscopy and Spectroscopy
11:03

Nanoscale Characterization of Liquid-Solid Interfaces by Coupling Cryo-Focused Ion Beam Milling with Scanning Electron Microscopy and Spectroscopy

Published on: July 14, 2022

相关实验视频

Last Updated: Jul 16, 2026

Fundamental Technical Elements of Freeze-fracture/Freeze-etch in Biological Electron Microscopy
11:17

Fundamental Technical Elements of Freeze-fracture/Freeze-etch in Biological Electron Microscopy

Published on: September 11, 2014

Studying the Supramolecular Organization of Photosynthetic Membranes within Freeze-fractured Leaf Tissues by Cryo-scanning Electron Microscopy
13:52

Studying the Supramolecular Organization of Photosynthetic Membranes within Freeze-fractured Leaf Tissues by Cryo-scanning Electron Microscopy

Published on: June 23, 2016

Nanoscale Characterization of Liquid-Solid Interfaces by Coupling Cryo-Focused Ion Beam Milling with Scanning Electron Microscopy and Spectroscopy
11:03

Nanoscale Characterization of Liquid-Solid Interfaces by Coupling Cryo-Focused Ion Beam Milling with Scanning Electron Microscopy and Spectroscopy

Published on: July 14, 2022

  • 已识别的dynein链接器提供了对运动蛋白精确协调的洞察力,以实现高效的运动性.
  • 这些发现有助于更深入地了解基底的分子机械真核细胞运动.