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 |
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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