The Department of Pharmacy, The First Affiliated Hospital of University of Science and Technology of China, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui 230001, China.
Hefei National Laboratory for Physical Sciences at the Microscale, Department of Polymer Science and Engineering, University of Science and Technology of China, Hefei, Anhui 230026, China.
ACS Appl Mater Interfaces. 2021 Dec 8;13(48):56838-56849. doi: 10.1021/acsami.1c15868. Epub 2021 Nov 24.
Antimicrobial resistance in Gram-negative bacteria has become one of the leading causes of morbidity and mortality and a serious worldwide public health concern due to the fact that Gram-negative bacteria have an additional outer membrane protecting them from an unwanted compound invading. It is still very difficult for antimicrobials to reach intracellular targets and very challenging to treat Gram-negative bacteria with the current strategies. Here, we found that (-(bromomethyl)phenyl)boronic acid was incorporated into poly((2--diethyl)aminoethyl acrylate) (PDEA), forming a copolymer (poly(-B-DEA)) having both phenylboronic acid (B) and ((2--diethyl)amino) (DEA) units. Poly(-B-DEA) exhibits very strong intramolecular B-N coordination, which could highly promote the covalent binding of phenylboronic acid with lipopolysaccharide (LPS) on the outer membrane of and lodge poly(-B-DEA) on the LPS layer on the surface of . Meanwhile, the strong electrostatic interaction between poly(-B-DEA) and the negatively charged lipid preferred tugging the poly(-B-DEA) into the lipid bilayer of . The combating interactions between covalent binding and electrostatic interaction form a tug-of-war action, which could trigger the lysis of the outer membrane, thereby killing Gram-negative effectively without detectable resistance.
革兰氏阴性菌的耐药性已成为发病率和死亡率的主要原因之一,也是全球严重的公共卫生关注问题,因为革兰氏阴性菌具有额外的外层膜,可保护其免受不受欢迎的化合物入侵。抗菌药物仍然很难到达细胞内靶标,并且用当前的策略治疗革兰氏阴性菌非常具有挑战性。在这里,我们发现(-(溴甲基)苯基)硼酸被掺入聚((2-二乙氨基)乙基丙烯酰胺)(PDEA)中,形成具有苯硼酸(B)和((2-二乙氨基)(DEA)单元的共聚物(聚(-B-DEA))。聚(-B-DEA)表现出非常强的分子内 B-N 配位,这可以高度促进苯硼酸与脂多糖(LPS)的共价结合,从而将聚(-B-DEA)固定在 的外膜上的 LPS 层上。同时,聚(-B-DEA)与带负电荷的脂质之间的强静电相互作用倾向于将聚(-B-DEA)拉入脂质双层中。共价结合和静电相互作用之间的对抗相互作用形成了拔河动作,这可以触发外膜的裂解,从而有效地杀死革兰氏阴性菌,而不会产生可检测的耐药性。