Design, Synthesis,and Biological Evaluation of Arginine N -GlycosylationStapled Peptides with Potent AntitumorActivity In Vivo

Abstract 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.