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7Q2R

cryo iDPC-STEM structure recorded with CSA 4.0

Summary for 7Q2R
Entry DOI10.2210/pdb7q2r/pdb
EMDB information13781
DescriptorCapsid protein, RNA (5'-R(P*GP*AP*A)-3') (2 entities in total)
Functional Keywordstobacco mosaic virus, rna virus, virus
Biological sourceTobacco mosaic virus (vulgare)
More
Total number of polymer chains2
Total formula weight18050.66
Authors
Sachse, C.,Leidl, M.L. (deposition date: 2021-10-26, release date: 2022-09-21, Last modification date: 2024-07-17)
Primary citationLazic, I.,Wirix, M.,Leidl, M.L.,de Haas, F.,Mann, D.,Beckers, M.,Pechnikova, E.V.,Muller-Caspary, K.,Egoavil, R.,Bosch, E.G.T.,Sachse, C.
Single-particle cryo-EM structures from iDPC-STEM at near-atomic resolution.
Nat.Methods, 19:1126-1136, 2022
Cited by
PubMed Abstract: In electron cryomicroscopy (cryo-EM), molecular images of vitrified biological samples are obtained by conventional transmission microscopy (CTEM) using large underfocuses and subsequently computationally combined into a high-resolution three-dimensional structure. Here, we apply scanning transmission electron microscopy (STEM) using the integrated differential phase contrast mode also known as iDPC-STEM to two cryo-EM test specimens, keyhole limpet hemocyanin (KLH) and tobacco mosaic virus (TMV). The micrographs show complete contrast transfer to high resolution and enable the cryo-EM structure determination for KLH at 6.5 Å resolution, as well as for TMV at 3.5 Å resolution using single-particle reconstruction methods, which share identical features with maps obtained by CTEM of a previously acquired same-sized TMV data set. These data show that STEM imaging in general, and in particular the iDPC-STEM approach, can be applied to vitrified single-particle specimens to determine near-atomic resolution cryo-EM structures of biological macromolecules.
PubMed: 36064775
DOI: 10.1038/s41592-022-01586-0
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.5 Å)
Structure validation

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