Structure-Property Relationship Study of N-(Hydroxy)Peptides for the Design of Self-Assembled Parallel β-Sheets.

17 June 2020, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

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.

Keywords

Peptide Foldamers
N-(hydroxy)peptides
Parallel beta-sheet
Peptide self-assembly
Hydrogen-bond network

Supplementary materials

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SI-Roche
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