Facial amphiphilicity index correlating chemical structures with antimicrobial efficacy

• Published in: Bioactive materials Vol. 20; pp. 519 - 527
• Main Authors: Buzoglu Kurnaz, Leman, Luo, Yuanyuan, Yang, Xiaoming, Alabresm, Amjed, Leighton, Ryan, Kumar, Rani, Hwang, JiHyeon, Decho, Alan W., Nagarkatti, Prakash, Nagarkatti, Mitzi, Tang, Chuanbing
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 01.02.2023; KeAi Publishing; KeAi Communications Co., Ltd
• Subjects: Antimicrobial; Chemical structure; Facial amphiphilicity; Peptide; Antimicrobial; Facial amphiphilicity; Peptide; Chemical structure
• ISSN: 2452-199X; 2452-199X
• DOI: 10.1016/j.bioactmat.2022.06.009

Facial amphiphilicity is an extraordinary chemical structure feature of a variety of antimicrobial peptides and polymers. Vast efforts have been dedicated to small molecular, macromolecular and dendrimer-like systems to mimic this highly preferred structure or conformation, including local facial amphiphilicity and global amphiphilicity. This work conceptualizes Facial Amphiphilicity Index (FAI) as a numerical value to quantitatively characterize the measure of chemical compositions and structural features in dictating antimicrobial efficacy. FAI is a ratio of numbers of charges to rings, representing both compositions of hydrophilicity and hydrophobicity. Cationic derivatives of multicyclic compounds were evaluated as model systems for testing antimicrobial selectivity against Gram-negative and Gram-positive bacteria. Both monocyclic and bicyclic compounds are non-antimicrobial regardless of FAIs. Antimicrobial efficacy was observed with systems having larger cross-sectional areas including tricyclic abietic acid and tetracyclic bile acid. While low and high FAIs respectively lead to higher and lower antimicrobial efficacy, in consideration of cytotoxicity, the sweet spot is typically suited with intermediate FAIs for each specific system. This can be well explained by the synergistic hydrophobic-hydrophobic and electrostatic interactions with bacterial cell membranes and the difference between bacterial and mammalian cell membranes. The adoption of FAI would pave a new avenue toward the design of next-generation antimicrobial macromolecules and peptides. [Display omitted] •Established a numerical index to quantify the effect of facial amphiphilicity on antimicrobial efficacy.•Evaluated the facial amphiphilicity index of multicyclic compounds possessing various rings and cationic charges.•Provided this index a new tool toward more quantitative designs of AMP mimics.