Department of Chemistry and Biochemistry, University of North Carolina Wilmington, Wilmington, NC, 28403, USA.
J Membr Biol. 2021 Feb;254(1):97-108. doi: 10.1007/s00232-021-00175-0. Epub 2021 Feb 23.
The mechanism of the antimicrobial peptide daptomycin is reviewed and discussed. Daptomycin is a last-resort antibiotic in current use against drug-resistant bacterial infections. Many models have been proposed for its function, most based on the observation that it increases membrane permeability and causes leakage of contents, such as ions and small molecules from bacterial cells and lipid vesicles. However, daptomycin is actually not efficient at permeabilizing or translocating across membranes, contrary to many well-known antimicrobial peptides. There is strong evidence that daptomycin binds preferentially to membranes in active division regions of bacterial cells and that it causes large membrane reorganization in terms of the distribution of lipids and proteins, both in cells and in model membranes. Those observations support the alternative hypothesis for the mechanism of daptomycin that its primary effect is in inducing membrane reorganization and that other events, such as increased membrane leakage and depolarization, are secondary consequences, not essential to its function.
本文回顾和讨论了抗菌肽达托霉素的作用机制。达托霉素是目前用于治疗耐药菌感染的最后手段抗生素。人们提出了许多关于其功能的模型,这些模型大多基于这样的观察结果,即它增加了细胞膜的通透性,并导致细菌细胞和脂质体中的离子和小分子等内容物泄漏。然而,与许多众所周知的抗菌肽不同,达托霉素实际上在透化或跨膜转运方面效率不高。有强有力的证据表明,达托霉素优先结合在细菌细胞活跃分裂区域的膜上,并且它导致脂质和蛋白质在细胞膜和模型膜中的分布发生大的重组。这些观察结果支持了达托霉素作用机制的替代假说,即其主要作用是诱导膜重组,而其他事件,如增加膜泄漏和去极化,是次要后果,对其功能并非必需。