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Author Notes:

Correspondence: egelman@virginia.edu

Acknowledgements: V.P.C. thanks Chunfu Xu for discussions on peptide design.

Subject:

Research Funding:

This work was supported by NIH R35GM122510 (to E.H.E.) and K99GM138756 (to F.W.), and NSF DMR-1534317 (to V.P.C.).

Keywords:

  • cryo-EM
  • synthetic soft matter non-covalent polymers
  • helical macromolecular assemblies

Cryo-EM of Helical Polymers

Tools:

Journal Title:

Chemical Review

Publisher:

Type of Work:

Article | Post-print: After Peer Review

Abstract:

While the application of 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 non-covalent 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 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.

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© 2022 American Chemical Society

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