Abstract
In electron cryo-microscopy (cryo-EM), the electron beam that is used for imaging also causes the sample to move. This motion blurs the images and limits the resolution attainable by single-particle analysis. In a previous Research article (Bai et al., 2013) we showed that correcting for this motion by processing movies from fast direct-electron detectors allowed structure determination to near-atomic resolution from 35,000 ribosome particles. In this Research advance article, we show that an improved movie processing algorithm is applicable to a much wider range of specimens. The new algorithm estimates straight movement tracks by considering multiple particles that are close to each other in the field of view, and models the fall-off of high-resolution information content by radiation damage in a dose-dependent manner. Application of the new algorithm to four data sets illustrates its potential for significantly improving cryo-EM structures, even for particles that are smaller than 200 kDa.
Keywords
cryo-EM
image analysis
single-particle analysis
MeSH Terms
Algorithms
Amyloid Precursor Protein Secretases/chemistry,ultrastructure
Animals
Cattle
Cryoelectron Microscopy/instrumentation,statistics & numerical data
Electron Transport Complex I/chemistry,ultrastructure
Escherichia coli/chemistry
Humans
Models, Molecular
Motion
Ribosomes/chemistry,ultrastructure
Saccharomyces cerevisiae/chemistry
beta-Galactosidase/chemistry,ultrastructure
Chemicals
beta-Galactosidase
Amyloid Precursor Protein Secretases
Electron Transport Complex I
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Scheres Sjors Hw
Structural Studies, Medical Research Council Laboratory of Molecular Biology, Cambridge, United Kingdom scheres@mrc-lmb.cam.ac.uk.
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