University of Sussex
Browse
Burgess_ja_2015_03973h_revision_markedup.pdf (15.02 MB)

Modular design of self-assembling peptide-based nanotubes

Download (15.02 MB)
journal contribution
posted on 2023-06-09, 00:48 authored by Natasha C Burgess, Thomas H Sharp, Franziska Thomas, Christopher W Wood, Andrew R Thomson, Nathan R Zaccai, R Leo Brady, Louise SerpellLouise Serpell, Derek N Woolfson
An ability to design peptide-based nanotubes (PNTs) rationally with defined and mutable internal channels would advance understanding of peptide self-assembly, and present new biomaterials for nanotechnology and medicine. PNTs have been made from Fmoc dipeptides, cyclic peptides, and lock-washer helical bundles. Here we show that blunt-ended a-helical barrels, that is, preassembled bundles of a-helices with central channels, can be used as building blocks for PNTs. This approach is general and systematic, and uses a set of de novo helical bundles as standards. One of these bundles, a hexameric a-helical barrel, assembles into highly ordered PNTs, for which we have determined a structure by combining cryo-transmission electron microscopy, X-ray fiber diffraction, and model building. The structure reveals that the overall symmetry of the peptide module plays a critical role in ripening and ordering of the supramolecular assembly. PNTs based on pentameric, hexameric, and heptameric a-helical barrels sequester hydrophobic dye within their lumens.

History

Publication status

  • Published

File Version

  • Accepted version

Journal

Journal of the American Chemical Society

ISSN

0002-7863

Publisher

American Chemical Society

Issue

33

Volume

137

Page range

10554-10562

Department affiliated with

  • Biochemistry Publications

Full text available

  • Yes

Peer reviewed?

  • Yes

Legacy Posted Date

2016-04-07

First Open Access (FOA) Date

2018-02-01

First Compliant Deposit (FCD) Date

2016-04-07

Usage metrics

    University of Sussex (Publications)

    Categories

    No categories selected

    Exports

    RefWorks
    BibTeX
    Ref. manager
    Endnote
    DataCite
    NLM
    DC