Modular Design of Self-Assembling Peptide-Based Nanotubes

Natasha C. Burgess(University of Bristol), Thomas H. Sharp(Leiden University Medical Center), Franziska Thomas(University of Bristol), Christopher W. Wood(University of Bristol), Andrew R. Thomson(University of Bristol), Nathan R. Zaccai(University of Bristol), R.L. Brady(University of Bristol), Louise C. Serpell(University of Sussex), Derek N. Woolfson(University of Bristol)
Journal of the American Chemical Society
July 28, 2015
Cited by 154Open Access
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Abstract

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 α-helical barrels, that is, preassembled bundles of α-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 α-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 α-helical barrels sequester hydrophobic dye within their lumens.


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