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Impact of Dehydroamino Acids on the Structure and Stability of Incipient 3₁₀ Helical Peptides

preprint
submitted on 10.10.2019, 23:04 and posted on 16.10.2019, 06:06 by Daniel Joaquin, Michael A. Lee, David W. Kastner, Jatinder Singh, Shardon T. Morrill, Gracie Damstedt, Steven Castle
A comparative study of the impact of small, medium-sized, and bulky Δ,Δ-dehydroamino acids (ΔAAs) on the structure and stability of Balaram’s incipient 3₁₀ -helical peptide (1) is reported. Replacement of the N-terminal Aib residue of 1 with a ΔAA afforded peptides 2a–c that maintained the 310-helical shape of 1 in solution. In contrast, installation of a ΔAA in place of Aib-3 yielded peptides 3a–c that preferred a Δ-sheet-like conformation. The impact of the ΔAA on peptide structure was independent of size, with small (ΔAla), medium-sized (Z-ΔAbu), and bulky (ΔVal) ΔAAs exerting similar effects. The proteolytic stabilities of 1 and its analogs were determined by incubation with Pronase. Z-ΔAbu and ΔVal increased the resistance of peptides to proteolysis when incorporated at the 3-position and had negligible impact on stability when placed at the 1-position, whereas ΔAla-containing peptides degraded rapidly regardless of position. Exposure of peptides 2a–c and 3a–c to the reactive thiol cysteamine revealed that ΔAla-containing peptides underwent conjugate addition at room temperature, while Z-ΔAbu- and ΔVal-containing peptides were inert even at elevated temperatures. These results suggest that both bulky and the more synthetically accessible medium-sized ΔAAs should be valuable tools for bestowing rigidity and proteolytic stability on bioactive peptides.

Funding

1R15GM114789-01A1

3R15GM114789-01A1S1

History

Email Address of Submitting Author

scastle@chem.byu.edu

Institution

Brigham Young University

Country

USA

ORCID For Submitting Author

0000-0002-7837-4964

Declaration of Conflict of Interest

The authors declare no conflicts of interest.

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