Structural Element of Vitamin U‐Mimicking Antibacterial Polypeptide with Ultrahigh Selectivity for Effectively Treating MRSA Infections

Abstract Antimicrobial peptides (AMPs) exhibit mighty antibacterial properties without inducing drug resistance. Achieving much higher selectivity of AMPs towards bacteria and normal cells has always been a continuous goal to be pursued. Herein, a series of sulfonium‐based polypeptides with different degrees of branching and polymerization were synthesized by mimicking the structure of vitamin U. The polypeptide, G 2 ‐PM‐1 H+ , shows both potent antibacterial activity and the highest selectivity index of 16000 among the reported AMPs or peptoids (e.g., the known index of 9600 for recorded peptoid in “Angew. Chem. Int. Ed ., 2020, 59, 6412.”), which can be attributed to the high positive charge density of sulfonium and the regulation of hydrophobic chains in the structure. The antibacterial mechanisms of G 2 ‐PM‐1 H+ are primarily ascribed to the interaction with the membrane, production of reactive oxygen species (ROS), and disfunction of ribosomes. Meanwhile, altering the degree of alkylation leads to selective antibacteria against either gram‐positive or gram‐negative bacteria in a mixed‐bacteria model. Additionally, both in vitro and in vivo experiments demonstrated that G 2 ‐PM‐1 H+ exhibited superior efficacy against methicillin‐resistant Staphylococcus aureus (MRSA) compared to vancomycin. Together, these results show that G 2 ‐PM‐1 H+ possesses high biocompatibility and is a potential pharmaceutical candidate in combating bacteria significantly threatening human health.