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. Author manuscript; available in PMC: 2017 Jun 1.
Published in final edited form as: Curr Protoc Nucleic Acid Chem. 2016 Jun 1;65:7.13.1–7.13.41. doi: 10.1002/cpnc.4

Table 7.13.2.

Electron Microscopy versus X-Ray Crystallography

Variable EM Crystallography
Sample size Relatively low amounts of material needed Milligram quantities required
Crystals No need for single crystals Crystallization constitutes a bottleneck on the way to structure determination
Molecular size Typically applied to large-size macromolecules or assemblies, (>300 kDa), but the technique has been successfully applied to a 78-kDa DNA nanostructure (Kato et al., 2009) No intrinsic size limitation (structures up to the MDa size range have been determined); however, large molecules can be difficult to crystallize
Resolution Typically 10 Å or less; but near-atomic resolution is possible (Zhou, 2008; Liu et al., 2010, Binshtein and Ohi, 2015; Rodriguez et al., 2015), and the number of cryo-EM structures with resolutions of 5 Å and higher is steadily increasing Near-atomic resolution can be achieved even with very large molecules, permitting detailed insights into recognition and mechanistic aspects