一本关于光片显微镜用于纳米尺度成像的实用指南:超越细胞的范围
Stephanie N Kramer1, Jeanpun Antarasen1, Cole R Reinholt1
1Department of Physics, Case Western Reserve University, Rockefeller Building, 2076 Adelbert Road, Cleveland, Ohio 44106, USA.
Journal of applied physics
|September 9, 2024
概括
本指南为科学家简化了光片显微镜 (LSM) 的实施. 它涵盖了基本概念,系统构建和数据分析,用于成像微尺度和纳米尺度的特征和扩散动态.
科学领域:
- 生物物理学的生物物理.
- 光学显微镜的使用方法
- 科学仪器仪表科学仪器仪表
背景情况:
- 光板显微镜 (LSM) 为成像动态生物过程提供了优势.
- 实施LSM,特别是定制构建的系统,给研究人员带来了重大的实际挑战.
- 需要一个清晰,易于阅读的指南,说明LSM的原则和构造.
研究的目的:
- 为光片显微镜的实际实施提供一个全面的指南.
- 协助科学家设计,构建和利用LSM系统.
- 作为一个有价值的资源,研究人员新的光片显微镜.
主要方法:
- 详细解释了与LSM相关的基本显微镜概念.
- 讨论光束形状的考虑和图像重建技术.
- 关于自制LSM系统的构建指南,包括对齐和校准.
主要成果:
- 概述了构建定制光板显微镜的实际决策.
- 提供了对关键对齐和校准程序的见解.
- 引入了自制代码,用于高效的数据分析.
结论:
- 这本指南揭开了光片显微镜实施的复杂性.
- 它使科学家能够克服在构建和运行LSM系统中的挑战.
- 促进了LSM的应用,用于成像静态和动态的微/纳米尺度现象.
相关概念视频
Imaging Biological Samples with Optical Microscopy
Optical microscopy uses optic principles to provide detailed images of samples. Antonie van Leeuwenhoek designed the first compound optical microscope in the 17th century to visualize blood cells, bacteria, and yeast cells. In 1830, Joseph Jackson Lister created an essentially modern light microscope. The 20th century saw the development of microscopes with enhanced magnification and resolution.
In optical microscopy, the specimen to be viewed is placed on a glass slide and clipped on the stage...
In optical microscopy, the specimen to be viewed is placed on a glass slide and clipped on the stage...
Confocal Fluorescence Microscopy
Confocal microscopy is an advanced microscopic technique. The prime advantage of the confocal microscope over other microscopy techniques is its ability to block the out-of-focus light from the illuminated samples using pinholes. It is widely used with fluorescence optics to obtain high-resolution, sharp contrast images. Unlike optical microscopes, confocal microscopes use a focused beam of light laser to scan the entire sample surface at different z-planes. These microscopes are, therefore,...
Super-resolution Fluorescence Microscopy
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 developed.
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.
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...
Three-Dimensional Microscopy in Microbiology
Three-dimensional imaging techniques are essential in cell biology, allowing researchers to visualize intricate cellular structures with high resolution. Two prominent methods, Differential Interference Contrast Microscopy (DIC) and Confocal Scanning Laser Microscopy (CSLM), provide distinct advantages for imaging live and thick specimens, respectively.Differential Interference Contrast MicroscopyDIC microscopy enhances contrast in transparent, unstained samples by converting phase...


