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.
Authors
- Robert W. Newberry (ORCID: https://orcid.org/0000-0002-2020-2641)
- Haoliang Zheng (ORCID: https://orcid.org/0000-0001-6241-4477)
Institutions
- The University of Texas at Austin (US)
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