Abstract
Lipid monolayers provide a convenient vehicle for the crystallization of biological macromolecules for 3-D electron microscopy. Although numerous examples of 3-D images from 2-D protein arrays have been described from negatively stained specimens, only six structures have been done from frozen-hydrated specimens. We describe here a method that makes high quality frozen-hydrated specimens of lipid monolayer arrays for cryoelectron microscopy. The method uses holey carbon films with patterned holes for monolayer recovery, blotting and plunge freezing to produce thin aqueous films which cover >90% of the available grid area. With this method, even specimens with relatively infrequent crystals can be screened using automated data collection techniques. Though developed for microscopic examination of 2-D arrays, the method may have wider application to the preparation of single particle specimens for 3-D image reconstruction.
MeSH Terms
Actinin/chemistry,ultrastructure
Animals
Carbon
Chickens
Cryoelectron Microscopy/methods
Crystallization/instrumentation,methods
Crystallography/instrumentation,methods
Freezing
Hydrophobic and Hydrophilic Interactions
Lipids/chemistry
Negative Staining/instrumentation,methods
Proteins/chemistry,ultrastructure
Specimen Handling/methods
Chemicals
Lipids
Proteins
Actinin
Carbon
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Taylor Dianne W
Institute of Molecular Biophysics, Florida State University, Tallahassee, FL 32306-4380, USA.
[email protected]
Kelly Deborah F
Cheng Anchi
Taylor Kenneth A
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