Design, Synthesis, and Biological Evaluation of Arginine N-Glycosylation Stapled Peptides with Potent Antitumor Activity In Vivo
- J Med Chem. 2025 Oct 9;68(19):20435-20448. doi: 10.1021/acs.jmedchem.5c01550.
- 1. School of Pharmaceutical Sciences & Institute of Materia Medica, State Key Laboratory of Advanced Drug Delivery and Release Systems, Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan, Shandong 250117, P. R. China.
- 2. Central Hospital Affiliated to Shandong First Medical University, Jinan, Shandong 250013, China.
- 3. School of Life Sciences, Medical Science and Technology Innovation Center, Shandong First Medical University & Shandong Academy of Medical Sciences, Tai'an 271016, China.
The host defense peptide PP-1 has attracted attention for its strong antitumor activity. However, its potential for clinical use is hindered by its poor proteolytic stability. In this study, a series of stapled PP-1 derivatives were obtained by an all-hydrocarbon stapling strategy and arginine N-glycosylation, and five rounds of peptide libraries containing more than 60 stapled and/or arginine N-glycosylated peptides were rationally constructed. PP-60 exhibited superior in vitro antitumor activities and low hemolytic toxicity. Compared with the parent peptide PP-1, PP-60 exhibited improved proteolytic and serum stability and, importantly, significantly weakened hemolysis and potential toxicity to liver tissue. Confocal microscopy revealed the superior cell permeability of PP-60. Flow cytometry revealed that PP-60 could exert its antitumor effects by inducing Apoptosis. Notably, PP-60 displayed a potent therapeutic effect without obvious side effects in a nude mouse model. PP-60 holds promise for further development as a lead antitumor agent.