Journal
JOURNAL OF STRUCTURAL BIOLOGY
Volume 200, Issue 3, Pages 307-313Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jsb.2017.02.009
Keywords
cryo-EM
Funding
- NIH [P01 GM051487, R01 GM065050, P41 GM103311]
- National Science Foundation Graduate Research Fellowship Program [1106400]
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Analysis of images of biotinylated Escherichia coli 70S ribosome particles, bound to streptavidin affinity grids, demonstrates that the image-quality of particles can be predicted by the image-quality of the monolayer crystalline support film. The quality of the Thon rings is also a good predictor of the image-quality of particles, but only when images of the streptavidin crystals extend to relatively high resolution. When the estimated resolution of streptavidin was 5 A or worse, for example, the ribosomal density map obtained from 22,697 particles went to only 9.5 A, while the resolution of the map reached 4.0 A for the same number of particles, when the estimated resolution of streptavidin crystal was 4 A or better. It thus is easy to tell which images in a data set ought to be retained for further work, based on the highest resolution seen for Bragg peaks in the computed Fourier transforms of the streptavidin component. The refined density map obtained from 57,826 particles obtained in this way extended to 3.6 A, a marked improvement over the value of 3.9 A obtained previously from a subset of 52,433 particles obtained from the same initial data set of 101,213 particles after 3-D classification. These results are consistent with the hypothesis that interaction with the air-water interface can damage particles when the sample becomes too thin. Streptavidin monolayer crystals appear to provide a good indication of when that is the case. (c) 2017 Elsevier Inc. All rights reserved.
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