How the spontaneous insertion of amphiphilic imidazolium-based cations changes biological membranes: a molecular simulation study

2015 ◽  
Vol 17 (43) ◽  
pp. 29171-29183 ◽  
Author(s):  
Geraldine S. Lim ◽  
Stephan Jaenicke ◽  
Marco Klähn

The insertion of 1-octyl-3-methylimidazolium cations (OMIM+) from a diluted aqueous ionic liquid (IL) solution into a model of a bacterial cell membrane is investigated.

RSC Advances ◽  
2015 ◽  
Vol 5 (81) ◽  
pp. 66476-66486 ◽  
Author(s):  
Dibyendu Das ◽  
Sumyra Sidiq ◽  
Santanu Kumar Pal

Liquid crystals offer a promising approach to study and quantify the interactions between different bacterial cell membrane components with endotoxin at an aqueous interface.


2005 ◽  
Vol 49 (3) ◽  
pp. 1127-1134 ◽  
Author(s):  
Deborah L. Higgins ◽  
Ray Chang ◽  
Dmitri V. Debabov ◽  
Joey Leung ◽  
Terry Wu ◽  
...  

ABSTRACTThe emergence and spread of multidrug-resistant gram-positive bacteria represent a serious clinical problem. Telavancin is a novel lipoglycopeptide antibiotic that possesses rapid in vitro bactericidal activity against a broad spectrum of clinically relevant gram-positive pathogens. Here we demonstrate that telavancin's antibacterial activity derives from at least two mechanisms. As observed with vancomycin, telavancin inhibited late-stage peptidoglycan biosynthesis in a substrate-dependent fashion and bound the cell wall, as it did the lipid II surrogate tripeptideN,N′-diacetyl-l-lysinyl-d-alanyl-d-alanine, with high affinity. Telavancin also perturbed bacterial cell membrane potential and permeability. In methicillin-resistantStaphylococcus aureus, telavancin caused rapid, concentration-dependent depolarization of the plasma membrane, increases in permeability, and leakage of cellular ATP and K+. The timing of these changes correlated with rapid , concentration-dependent loss of bacterial viability, suggesting that the early bactericidal activity of telavancin results from dissipation of cell membrane potential and an increase in membrane permeability. Binding and cell fractionation studies provided direct evidence for an interaction of telavancin with the bacterial cell membrane; stronger binding interactions were observed with the bacterial cell wall and cell membrane relative to vancomycin. We suggest that this multifunctional mechanism of action confers advantageous antibacterial properties.


2012 ◽  
Vol 14 (15) ◽  
pp. 5200 ◽  
Author(s):  
György Hantal ◽  
Iuliia Voroshylova ◽  
M. Natália D. S. Cordeiro ◽  
Miguel Jorge

2010 ◽  
Vol 5 (3) ◽  
pp. 355-358 ◽  
Author(s):  
Esteban C Nannini ◽  
Martin E Stryjewski ◽  
G Ralph Corey

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