| Literature DB >> 31518065 |
John R Gallagher1, Alexander J Kim1, Neetu M Gulati1, Audray K Harris1.
Abstract
Negative-stain transmission electron microscopy (EM) is a technique that has provided nanometer resolution images of macromolecules for about 60 years. Developments in cryo-EM image processing have maximized the information gained from averaging large numbers of particles. These developments can now be applied back to negative-stain image analysis to ascertain domain level molecular structure (10 to 20 Å) more quickly and efficiently than possible by atomic resolution cryo-EM. Using uranyl acetate stained molecular complexes of influenza hemagglutinin bound to Fab 441D6, we describe a simple and efficient means to collect several hundred micrographs with SerialEM. Using RELION, we illustrate how tens of thousands of complexes can be auto-picked and classified to accurately describe the domain level topology of this unconventional hemagglutinin head-domain epitope. By comparing to the cryo-EM density map of the same complex, we show that questions about epitope mapping and conformational heterogeneity can readily be answered by this negative-stain method.Entities:
Keywords: electron microscopy; image analysis; image processing; negative stain
Mesh:
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Year: 2019 PMID: 31518065 PMCID: PMC6746251 DOI: 10.1002/cpmc.90
Source DB: PubMed Journal: Curr Protoc Microbiol ISSN: 1934-8525