7rx5 | pdb_00007rx5
From Proteopedia
Cryo-EM reconstruction of Form1-N2 nanotube (Form I like)
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Structural highlights
Publication Abstract from PubMedWhile the application of cryogenic electron microscopy (cryo-EM) to helical polymers in biology has a long history, due to the huge number of helical macromolecular assemblies in viruses, bacteria, archaea, and eukaryotes, the use of cryo-EM to study synthetic soft matter noncovalent polymers has been much more limited. This has mainly been due to the lack of familiarity with cryo-EM in the materials science and chemistry communities, in contrast to the fact that cryo-EM was developed as a biological technique. Nevertheless, the relatively few structures of self-assembled peptide nanotubes and ribbons solved at near-atomic resolution by cryo-EM have demonstrated that cryo-EM should be the method of choice for a structural analysis of synthetic helical filaments. In addition, cryo-EM has also demonstrated that the self-assembly of soft matter polymers has enormous potential for polymorphism, something that may be obscured by techniques such as scattering and spectroscopy. These cryo-EM structures have revealed how far we currently are from being able to predict the structure of these polymers due to their chaotic self-assembly behavior. Cryo-EM of Helical Polymers.,Wang F, Gnewou O, Solemanifar A, Conticello VP, Egelman EH Chem Rev. 2022 Feb 8. doi: 10.1021/acs.chemrev.1c00753. PMID:35133794[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. References
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This page was last modified 07:31, 2 March 2022.