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TitleHigh-resolution electron microscopy of helical specimens: a fresh look at tobacco mosaic virus.
Journal, issue, pagesJ Mol Biol, Vol. 371, Issue 3, Page 812-835, Year 2007
Publish dateAug 17, 2007
AuthorsCarsten Sachse / James Z Chen / Pierre-Damien Coureux / M Elizabeth Stroupe / Marcus Fändrich / Nikolaus Grigorieff /
PubMed AbstractThe treatment of helical objects as a string of single particles has become an established technique to resolve their three-dimensional (3D) structure using electron cryo-microscopy. It can be ...The treatment of helical objects as a string of single particles has become an established technique to resolve their three-dimensional (3D) structure using electron cryo-microscopy. It can be applied to a wide range of helical particles such as viruses, microtubules and helical filaments. We have made improvements to this approach using Tobacco Mosaic Virus (TMV) as a test specimen and obtained a map from 210,000 asymmetric units at a resolution better than 5 A. This was made possible by performing a full correction of the contrast transfer function of the microscope. Alignment of helical segments was helped by constraints derived from the helical symmetry of the virus. Furthermore, symmetrization was implemented by multiple inclusions of symmetry-related views in the 3D reconstruction. We used the density map to build an atomic model of TMV. The model was refined using a real-space refinement strategy that accommodates multiple conformers. The atomic model shows significant deviations from the deposited model for the helical form of TMV at the lower-radius region (residues 88 to 109). This region appears more ordered with well-defined secondary structure, compared with the earlier helical structure. The RNA phosphate backbone is sandwiched between two arginine side-chains, stabilizing the interaction between RNA and coat protein. A cluster of two or three carboxylates is buried in a hydrophobic environment isolating it from neighboring subunits. These carboxylates may represent the so-called Caspar carboxylates that form a metastable switch for viral disassembly. Overall, the observed differences suggest that the new model represents a different, more stable state of the virus, compared with the earlier published model.
External linksJ Mol Biol / PubMed:17585939 / PubMed Central
MethodsEM (helical sym.)
Resolution4.4 Å
Structure data

EMDB-1316: High-resolution electron microscopy of helical specimens: a fresh look at tobacco mosaic virus.
PDB-2om3: High-resolution cryo-EM structure of Tobacco Mosaic Virus
Method: EM (helical sym.) / Resolution: 4.4 Å

Source
  • tobacco mosaic virus
KeywordsVIRUS / protein-RNA complex / four-helical up-and-down bundle / HELICAL VIRUS

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