Thioamides in C5 Hydrogen Bonds: Implications for Protein β-Strands

Though thioamides are considered weaker hydrogen-bond acceptors than oxoamides, recent calculations suggest that they can 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 highlights opportunities to control β-strand stability.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-09-18
DOI
https://doi.org/10.1021/acs.joc.5c01310
Citations
2
Primary Topic
Protein Structure and Dynamics
Type
article
Field-Weighted Citation Impact
1.61
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article

Thioamides in C5 Hydrogen Bonds: Implications for Protein β-Strands

Robert W. Newberry, Haoliang Zheng
2 citations
The Journal of Organic Chemistry
Protein Structure and Dynamics
1.61
article

Thioamides in C5 Hydrogen Bonds: Implications for Protein β-Strands

Robert W. Newberry, Haoliang Zheng
article en
2 citations

Abstract

Though thioamides are considered weaker hydrogen-bond acceptors than oxoamides, recent calculations suggest that they can 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 highlights opportunities to control β-strand stability.

The Journal of Organic ChemistryVol. 90(39)
The University of Texas at Austin (US)
Openalex Percentile: Top 15%
Protein Structure and Dynamics
1.61
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Thioamides in C5 Hydrogen Bonds: Implications for Protein β-Strands — Robert W. Newberry, Haoliang Zheng · The Journal of Organic Chemistry (2025) | TGRS Research Map | TGRS