TY - JOUR
T1 - Modular design of self-assembling peptide-based nanotubes
AU - Burgess, Natasha C.
AU - Sharp, Thomas H.
AU - Thomas, Franziska
AU - Wood, Christopher W.
AU - Thomson, Andrew R.
AU - Zaccai, Nathan R.
AU - Brady, R. Leo
AU - Serpell, Louise C.
AU - Woolfson, Derek N.
PY - 2015/7/28
Y1 - 2015/7/28
N2 - 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.
AB - 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.
U2 - 10.1021/jacs.5b03973
DO - 10.1021/jacs.5b03973
M3 - Article
C2 - 26219086
AN - SCOPUS:84941687391
SN - 0002-7863
VL - 137
SP - 10554
EP - 10562
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 33
ER -