通过低能电子全息学在单个分子水平上对全息素和阿波转移素的成像构造图像
Hannah Ochner1, Sven Szilagyi2, Moritz Edte2
1Max Planck Institute for Solid State Research, Heisenbergstr. 1, 70569, Stuttgart, Germany. h.ochner@fkf.mpg.de.
Scientific reports
|June 23, 2023
概括
低能电子全息 (LEEH) 可以对单个蛋白质的结构变化进行成像. 这种技术成功地可视化了转激素的独特结构,揭示了它与功能相关的灵活性.
科学领域:
- 结构生物学 结构生物学
- 生物物理学的生物物理.
背景情况:
- 蛋白质的结构变化对于生物功能至关重要.
- 在单个分子水平上对这些动态变化的成像至关重要.
- 之前的研究集中在环境诱导的变化.
研究的目的:
- 评估低能电子全息 (LEEH) 用于成像功能相关的蛋白质构造变化.
- 为了研究铁运输蛋白质转激素的构造空间.
主要方法:
- 低能电子全息 (LEEH) 与原生电喷射离子束沉积 (ES-IBD) 相结合.
- 转移林的单分子成像.
- 分子灵活性的统计分析.
主要成果:
- 李成功地区分了不同形状的转移蛋白.
- 解决了与铁结合相关的阿波-转移蛋白中的纳米尺度裂.
- 数据分析证实了分子灵活性.
结论:
- 李 (LEEH) 是一种可行的技术,用于成像单个蛋白质的功能相关的构造变化.
- 这项研究证明了LEEH在探索与生物功能相关的蛋白质动态方面的能力.
相关概念视频
Electron Microscope Tomography and Single-particle Reconstruction
2.4K
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...
2.4K
Cryo-electron Microscopy
3.4K
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...
3.4K
Total Internal Reflection Fluorescence Microscopy
5.9K
Total internal reflection fluorescence microscopy or TIRF is an advanced microscopic technique used to visualize fluorophores in samples close to a solid surface with a higher refractive index, such as a glass coverslip. TIRF only allows fluorophores in proximity to the solid surface to be excited. When light from a medium with a lower refractive index (such as air) hits the glass coverslip at a critical angle, the light undergoes total internal reflection stead of passing through the glass.
5.9K


