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Please use this identifier to cite or link to this item: http://apo.ansto.gov.au/dspace/handle/10238/6236

Title: Asymmetric phospholipid: lipopolysaccharide bilayers; a Gram-negative bacterial outer membrane mimic
Authors: Clifton, LA
Skoda, MWA
Daulton, EL
Hughes, AV
Le Brun, AP
Lakey, JH
Holt, SA
Keywords: BACTERIA
IN VIVO
LIPIDS
BACTERIA
MEMBRANES
ESCHERICHIA COLI
Issue Date: 16-Oct-2013
Publisher: The Royal Society
Citation: Clifton, L. A., Skoda, M. W. A., Daulton, E. L., Hughes, A. V., Le Brun, A. P., Lakey, J. H., . . . Holt, S. A. (2013). Asymmetric phospholipid: lipopolysaccharide bilayers; a Gram-negative bacterial outer membrane mimic. Journal of the Royal Society Interface, 10(89).
Abstract: The Gram-negative bacterial outer membrane (OM) is a complex and highly asymmetric biological barrier but the small size of bacteria has hindered advances in in vivo examination of membrane dynamics. Thus, model OMs, amenable to physical study, are important sources of data. Here, we present data from asymmetric bilayers which emulate the OM and are formed by a simple two-step approach. The bilayers were deposited on an SiO2 surface by Langmuir–Blodgett deposition of phosphatidylcholine as the inner leaflet and, via Langmuir–Schaefer deposition, an outer leaflet of either Lipid A or Escherichia coli rough lipopolysaccharides (LPS). The membranes were examined using neutron reflectometry (NR) to examine the coverage and mixing of lipids between the bilayer leaflets. NR data showed that in all cases, the initial deposition asymmetry was mostly maintained for more than 16 h. This stability enabled the sizes of the headgroups and bilayer roughness of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine and Lipid A, Rc-LPS and Ra-LPS to be clearly resolved. The results show that rough LPS can be manipulated like phospholipids and used to fabricate advanced asymmetric bacterial membrane models using well-known bilayer deposition techniques. Such models will enable OM dynamics and interactions to be studied under in vivo-like conditions. © 2013, The Royal Society.
URI: http://dx.doi.org/10.1098/rsif.2013.0810
http://apo.ansto.gov.au/dspace/handle/10238/6236
ISSN: 1742-5662
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