Gazerani Golbarg, Piercey Lesley R, Reema Syeda, Wilson Katie A
Department of Biochemistry, Memorial University of Newfoundland, St. John's, Newfoundland and Labrador A1C 5S7, Canada.
J Chem Inf Model. 2025 Feb 10;65(3):1453-1464. doi: 10.1021/acs.jcim.4c01457. Epub 2025 Jan 28.
The World Health Organization has identified multidrug-resistant bacteria as a serious global health threat. Gram-negative bacteria are particularly prone to antibiotic resistance, and their high rate of antibiotic resistance has been suggested to be related to the complex structure of their cell membrane. The outer membrane of Gram-negative bacteria contains lipopolysaccharides that protect the bacteria against threats such as antibiotics, while the inner membrane houses 20-30% of the bacterial cellular proteins. Given the cell membrane's critical role in bacterial survival, antibiotics targeting the cell membrane have been proposed to combat bacterial infections. However, a deeper understanding of the biophysical properties of the bacterial cell membrane is crucial to developing effective and specific antibiotics. In this study, Martini coarse-grain molecular dynamics simulations were used to investigate the interplay between membrane composition and biophysical properties of the inner membrane across four pathogenic bacterial species: , , , and . The simulations indicate the impact of species-specific membrane composition on the overall membrane properties. Specifically, the cardiolipin concentration in the inner membrane is a key factor influencing the membrane features. Model membranes with varying concentrations of bacterial lipids (phosphatidylglycerol, phosphatidylethanolamine, and cardiolipin) further support the significant role of cardiolipin in determining the membrane biophysical properties. The bacterial inner membrane models developed in this work pave the way for future simulations of bacterial membrane proteins and for simulations investigating novel strategies aimed at disrupting the bacterial membrane to treat antibiotic-resistant infections.
世界卫生组织已将多重耐药细菌确定为严重的全球健康威胁。革兰氏阴性菌尤其容易产生抗生素耐药性,其高抗生素耐药率被认为与细胞膜的复杂结构有关。革兰氏阴性菌的外膜含有脂多糖,可保护细菌免受抗生素等威胁,而内膜则容纳了20%至30%的细菌细胞蛋白质。鉴于细胞膜在细菌存活中的关键作用,已有人提出靶向细胞膜的抗生素来对抗细菌感染。然而,深入了解细菌细胞膜的生物物理特性对于开发有效且特异性的抗生素至关重要。在本研究中,使用马尔蒂尼粗粒度分子动力学模拟来研究四种致病细菌物种( 、 、 和 )的内膜膜组成与生物物理特性之间的相互作用。模拟结果表明物种特异性膜组成对整体膜特性的影响。具体而言,内膜中的心磷脂浓度是影响膜特征的关键因素。含有不同浓度细菌脂质(磷脂酰甘油、磷脂酰乙醇胺和心磷脂)的模型膜进一步支持了心磷脂在决定膜生物物理特性方面的重要作用。这项工作中开发的细菌内膜模型为未来细菌膜蛋白的模拟以及研究旨在破坏细菌膜以治疗抗生素耐药感染的新策略的模拟铺平了道路。