biostudies-literatureLiao FHMinistry of Science and Technology, TaiwanNational Health Research Institutes1430-1434https://www.ebi.ac.uk/biostudies/studies/S-EPMC7687082biostudies-literatureUnknown59(4)A strong interaction between colistin, a last-resort antibiotic of the polymyxin family, and free lipopolysaccharide (LPS, also referred to as endotoxin), released from the Gram-negative bacterial (GNB) outer membrane (OM), has been identified that can decrease the antibacterial efficacy of colistin, potentially increasing the dose of this antibiotic required for treatment. The competition between LPS in the GNB OM and free LPS for the interaction with colistin was prevented by using a supramolecular trap to capture free LPS. The supramolecular trap, fabricated from a subnanometer gold nanosheet with methyl motifs (SAuM), blocks lipid A, preventing the interaction between lipid A and colistin. This can minimize endotoxemia and maximize the antibacterial efficacy of colistin, enabling colistin to be used at lower doses. Thus, the potential crisis of colistin resistance could be avoided.Angewandte Chemie (International ed. in English)A Supramolecular Trap to Increase the Antibacterial Activity of Colistin.PMC7687082MOST-106-2113-M-400-005-MY3NHRI-BN-107-PP-30Su CJKuo SCLiao FHWu THYao CNJeng USLin SYfalseA Supramolecular Trap to Increase the Antibacterial Activity of Colistin.A strong interaction between colistin, a last-resort antibiotic of the polymyxin family, and free lipopolysaccharide (LPS, also referred to as endotoxin), released from the Gram-negative bacterial (GNB) outer membrane (OM), has been identified that can decrease the antibacterial efficacy of colistin, potentially increasing the dose of this antibiotic required for treatment. The competition between LPS in the GNB OM and free LPS for the interaction with colistin was prevented by using a supramolecular trap to capture free LPS. The supramolecular trap, fabricated from a subnanometer gold nanosheet with methyl motifs (SAuM), blocks lipid A, preventing the interaction between lipid A and colistin. This can minimize endotoxemia and maximize the antibacterial efficacy of colistin, enabling colistin to be used at lower doses. Thus, the potential crisis of colistin resistance could be avoided.2020-01-01T00:00:00Z2020 Jan2024-12-04T09:43:53.274Z2021-02-20T02:54:49ZS-EPMC76870823172910610.1002/anie.201912137