Unusual Directionality in Thioamide Hydrogen Bonds Can Stabilize β-Strands

01 October 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Though thioamides are considered weaker hydrogen-bond acceptors than oxoamides, recent calculations suggest they might enhance hydrogen bonds within the backbone of individual β-strands. We confirm this prediction through spectroscopic analysis of minimal amino-acid models. Further, incorporation of thioamides into the backbone of β-hairpin models high-lights opportunities to control β-strand stability.

Keywords

Thioamide
Hydrogen bond
Protein structure

Supplementary materials

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Supporting information
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Synthetic and analytical methods, characterization data for small molecules and peptides.
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