Related Experiment Video
Updated: Aug 11, 2026

08:04
Preparation and Observation of Thick Biological Samples by Scanning Transmission Electron Tomography
Published on: March 12, 2017
Special specimen preparation methods for image processing in transmission electron microscopy: a review
Journal of Microscopy
|August 1, 1978
Summary
Researchers review in vitro formation of viral crystalline arrays. This technique enhances image analysis in electron microscopy for studying virus assembly and dissociation.
Area of Science:
- Quantitative electron microscopy
- Biophysical imaging techniques
Background:
- Image analysis of electron micrographs is crucial for quantitative microscopy.
- Current methods often analyze isolated biological structures with negative stains.
- Limited naturally occurring specimens exhibit crystalline features suitable for high-resolution analysis.
Purpose of the Study:
- To review in vitro formation of crystalline and paracrystalline arrays from purified viruses.
- To discuss challenges in preparing 2D and 3D crystalline arrays.
- To explore extending negative staining for studying viral component dynamics.
Main Methods:
- In vitro formation of crystalline and paracrystalline arrays from purified isometric, filamentous, and rod-like viruses.
- Application of optical and computer imaging methods to electron micrographs.
- Utilizing negative staining with carbon film techniques.
Main Results:
- Successful in vitro formation of ordered viral arrays from various virus types.
- Identification of preparative challenges for producing 2D and 3D crystalline structures.
- Demonstrated potential for studying dynamic viral assembly/dissociation processes.
Conclusions:
- In vitro formation of viral crystalline arrays offers a viable alternative to limited natural specimens.
- Advanced image processing techniques can be applied to these arrays for detailed structural analysis.
- The negative staining-carbon film method can be adapted to observe dynamic viral processes.
More Related Videos
Related Concept Videos
Fixation and Sectioning
Two basic types of preparation are used to visualize specimens with a light microscope: wet mounts and fixed specimens.
The simplest type of preparation is the wet mount, in which the specimen is placed in a drop of liquid on the slide. A liquid specimen can be directly deposited on the slide using a dropper. Solid specimens, such as skin scraping, can be placed on the slide before adding a drop of liquid to prepare the wet mount. Sometimes the liquid is simply water, but stains are often added...
The simplest type of preparation is the wet mount, in which the specimen is placed in a drop of liquid on the slide. A liquid specimen can be directly deposited on the slide using a dropper. Solid specimens, such as skin scraping, can be placed on the slide before adding a drop of liquid to prepare the wet mount. Sometimes the liquid is simply water, but stains are often added...
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.
Transmission Electron Microscopy
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 keV in...
Preparation of Samples for Electron Microscopy
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...
Immunogold Electron Microscopy
Immunoelectron microscopy utilizes immunogold labeling of endogenous proteins with specific antibodies to detect and localize these proteins in cells and tissues. The procedure provides insights into the distribution and quantification of protein under different stimulation conditions offering clues about their functions. Conjugating highly electron-dense gold particles with primary or secondary antibodies allow antigen detection on and within cells, with high resolution and specificity.

