Abstract
The N-capping box is a distinct helix-stabilizing motif frequently found in proteins. In this study, we examined a ruthenium-mediated intramolecular backbone to side chain macrocyclization as a rigidified mimicry of the N-capping box. Experimental data indicate that the 15-membered macrocycle formed by a hept-4-enoyl staple, which directly tethers the α-amino group of N1 residue and the α-carbon of N3 residue, is highly effective in stabilizing helical structures of short peptides.
| Original language | English |
|---|---|
| Article number | 104024 |
| Journal | Bioorganic Chemistry |
| Volume | 101 |
| DOIs | |
| State | Published - Aug 2020 |
Keywords
- N-capping box
- Peptide drugs
- Peptide stapling
- Ring-closing metathesis
- α-Helix