Journal
STRUCTURE
Volume 13, Issue 3, Pages 355-362Publisher
CELL PRESS
DOI: 10.1016/j.str.2005.01.005
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The combination of cryo-electron microscopy to study large biological assemblies at low resolution with crystallography to determine near atomic structures of assembly fragments is quickly expanding the horizon of structural biology. This technique can be used to advantage in the study of large structures that cannot be crystallized, to follow dynamic processes, and to purify samples by visual selection of particles. Factors affecting the quality of cryo-electron microscopy maps and limits of accuracy in fitting known structural fragments are discussed.
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