Abstract
AbstractCryoEM is a powerful tool in the arsenal of structural biologists and soft polymer chemists. Hydrated specimens require a preservation method that will counteract the effects of the electron beam and the high vacuum environment of the electron microscope. Classical specimen preparation techniques using chemical fixatives are not able to capture the native structure of the once hydrated specimen perfectly. In contrast to classical methods for preserving specimens for electron microscopy, rapid freezing of radiation-sensitive specimens such as dispersed biological macromolecular assemblies, 2D crystals, and colloids allows the structural details of the specimen to be captured in their essentially native state to near atomic resolution.
References
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Dates
Type | When |
---|---|
Created | 7 years, 2 months ago (May 22, 2018, 10:20 a.m.) |
Deposited | 1 year, 1 month ago (July 6, 2024, 6:40 p.m.) |
Indexed | 1 year, 1 month ago (July 6, 2024, 7:40 p.m.) |
Issued | 16 years, 5 months ago (March 1, 2009) |
Published | 16 years, 5 months ago (March 1, 2009) |
Published Online | 7 years, 5 months ago (March 14, 2018) |
Published Print | 16 years, 5 months ago (March 1, 2009) |
@article{Melanson_2009, title={A Versatile and Affordable Plunge Freezing Instrument for Preparing Frozen Hydrated Specimens for Cryo Transmission Electron Microscopy (CryoEM)}, volume={17}, ISSN={1551-9295}, url={http://dx.doi.org/10.1017/s1551929500054432}, DOI={10.1017/s1551929500054432}, number={2}, journal={Microscopy Today}, publisher={Oxford University Press (OUP)}, author={Melanson, Linda}, year={2009}, month=mar, pages={14–17} }