Coarse-grained simulations uncover Gram-negative bacterial defense against polymyxins by the outer membrane
[Display omitted] •A structural model of bacterial outer membrane (OM) was developed with Ra LPS.•Free energy landscape was revealed for polymyxin interactions with the OM.•LPS core sugars and calcium ions confer intrinsic resistance to antibiotics. The outer membrane (OM) of Gram-negative bacteria...
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Veröffentlicht in: | Computational and structural biotechnology journal 2021-01, Vol.19, p.3885-3891 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
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•A structural model of bacterial outer membrane (OM) was developed with Ra LPS.•Free energy landscape was revealed for polymyxin interactions with the OM.•LPS core sugars and calcium ions confer intrinsic resistance to antibiotics.
The outer membrane (OM) of Gram-negative bacteria is a formidable barrier against antibiotics. Understanding the structure and function of the OM is essential for the discovery of novel membrane-acting agents against multidrug-resistant Gram-negative pathogens. However, it remains challenging to obtain three-dimensional structure of bacterial membranes using crystallographic approaches, which has significantly hindered the elucidation of its interaction with antibiotics. Here, we developed an asymmetric OM model consisting of rough lipopolysaccharide (LPS) and three key types of phospholipids. Using coarse-grained molecular dynamics simulations, we investigated the interaction dynamics of LPS-containing OM with the polymyxins, a last-line class of antibiotics against Gram-negative ‘superbugs’. We discovered that polymyxin molecules spontaneously penetrated the OM core sugar region where most were trapped before entering the lipid A region. Examination of the free energy profile of polymyxin penetration revealed a major free energy barrier at the LPS inner core and lipid A interface. Further analysis revealed calcium ions predominantly distributed in the inner core region and mediated extensive cross-linking interactions between LPS molecules, thereby inhibiting the penetration of polymyxins into the hydrophobic region of the OM. Collectively, our results provide novel mechanistic insights into an intrinsic defense of Gram-negative bacteria to polymyxins and may help identify new antimicrobial targets. |
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ISSN: | 2001-0370 2001-0370 |
DOI: | 10.1016/j.csbj.2021.06.051 |