electron microscopy (EM)
Jump to navigation
Jump to search
Classification
- EM techniques can be roughly divided into two main modalities which each require differently designed electron microscopes
- transmission EM
- an electron beam >= width of the field of view penetrates the sample
- electrons transmitted through the sample create a projection image captured by a detector
- samples are 100-300 nm, due to limited penetration depth of the electron beam
- specimen is gradually tilted to generate a series of 2D projection images at different angles
- these projections can be computationally aligned & combined into a tomographic volume
- the tilt angle is restricted to a maximum of ~70 degrees[1]
- scanning EM
- a focused electron beam scans the surface of the sample
- backscattered electrons are collected by a detector situated above the sample
- can be applied to larger specimens & larger fields of view than transmission EM
- whole cells & specific areas in a cell may be analyzed
- cryotomography is used to image the biological content in a near-native state
- allows the direct visualization of macromolecular complexes like ribosomes & polysomes, clathrin coats, ATP synthases, & individual tubulin subunits in microtubules[1]
- transmission EM
Clinical significance
- resolution ~100 higher than light microscopy
- enables visualization of previously invisible virus particles
More general terms
More specific terms
- abnormal prion protein in brain by electron microscopy
- microscopic observation in stool by electron microscopy
- microscopic observation in tissue by electron microscopy
- platelet dense bodies in blood by electron microscopy
References
- ↑ 1.0 1.1 1.2 Wolff G, Barcena M Multiscale Electron Microscopy for the Study of Viral Replication Organelles. Viruses. 2021 Jan 28;13(2):197. PMID: https://www.ncbi.nlm.nih.gov/pubmed/33525547 PMCID: PMC7912242 Free PMC article