Abstract
The design of novel and functional biomimetic
foldamers remains a major challenge in creating mimics of native protein
structures. Herein, we report the stabilization of a short b-sheet by incorporating N-(hydroxy)glycine (Hyg) residues into the backbone of peptides.
These short peptide−peptoid hybrids form unique parallel b-sheet structures by self-assembly.
Spectroscopic and crystallographic data collected suggest that the local
conformational perturbations induced by N-(hydroxy)amides
are outweighed by a network of strong interstrand hydrogen-bonds.
Supplementary materials
Title
SI-Roche
Description
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