Assessment of structural features in Cryo-EM density maps using SSE and side chain Z-scores

J Struct Biol. 2018 Dec;204(3):564-571. doi: 10.1016/j.jsb.2018.08.015. Epub 2018 Aug 23.

Abstract

We introduce a new method for assessing resolvability of structural features in density maps from Cryo-Electron Microscopy (Cryo-EM) using fitted or derived models. It calculates Z-scores for secondary structure elements (SSEs) and side chains. Z-scores capture how much larger the cross-correlation score (CCS) is for atoms in such features at their placed locations compared to the CCS at displaced positions. Z-scores are larger when the structural features are well-resolved, as confirmed by visual analysis. This method was applied to all 66 maps submitted to the 2015/2016 EMDB map challenge. For each map, the fitted model provided by the map committee was used in this assessment. The average Z-scores for each map and fitted model correlate moderately well with reported map resolutions (r2 = 0.45 for SSE Z-scores and r2 = 0.56 for side chain Z-scores). Rankings of the submitted maps based on average Z-scores seem to more closely agree with visual analysis. Z-scores can also be used to pinpoint which parts of a model are well-resolved in a map, and which parts of the model may need further fitting or refinement to make the model better match the density.

Keywords: Cryo-Electron Microscopy; Proteins; Secondary structures; Side chains; Statistics.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Cryoelectron Microscopy / methods*
  • Models, Molecular
  • Proteasome Endopeptidase Complex / chemistry
  • Proteasome Endopeptidase Complex / ultrastructure
  • Protein Conformation*
  • Protein Structure, Secondary*
  • Proteins / chemistry*
  • Proteins / ultrastructure

Substances

  • Proteins
  • Proteasome Endopeptidase Complex