Journal
JOURNAL OF PHYSICAL CHEMISTRY B
Volume 120, Issue 43, Pages 11170-11179Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcb.6b06615
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Funding
- EPSRC [EP/L000253/1]
- Engineering and Physical Sciences Research Council [EP/L000253/1] Funding Source: researchfish
- EPSRC [EP/L000253/1] Funding Source: UKRI
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Carbon fullerenes are emerging as effective devices for different biomedical applications, including the transportation of nanosized drugs and extraction of harmful oxidants and radicals. It has been proposed that fullerenes could be used as novel antibacterial agents, given the realization that the nanoparticles can kill pathogenic Gram-negative bacteria. To explore this at the molecular level, we simulated C-60 fullerenes with bacterial membranes using the coarse-grain molecular dynamics Martini force field. We found that pristine C-60 has a limited tendency to penetrate (incomplete core) Re mutant lipopolysaccharide (LPS) leaflets, but the translocation of C-60 fullerenes into (complete core) Ra mutant LPS leaflets is not thermodynamically favored. Moreover, we showed that the permeability of the Re LPS bilayers depends sensitively on the system temperature, charge of ambient ions, and prevalence of palmitoyloleoylphosphoethanolamine (POPE) defect domains. The different permeabilities are rationalized in terms of transitory head group pore formation, which underpins the translocation of C-60 into the lipid core. The Re LPS lipids readily form transient micropores when they are linked with monovalent cations or when they are heated to a high temperature. POPE lipids are shown to be particularly adept at forming these transient surface cavities, and their inclusion into Re LPS membranes facilitates the formation of particularly large pores that are tunneled by C-60 aggregates of a significant size (similar to 5 nm wide). After insertion into the lipid core, the aggregates dissociate, and the disbanded nanoparticles migrate to the interface between separate POPE and LPS domains, where they weaken the boundaries between the coexisting lipid fractions and thereby promote lipid mixing.
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