Browse by author
Lookup NU author(s): Anton Le Brun,
Professor Jeremy LakeyORCiD
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
© 2016 Elsevier B.V. All rights reserved. Studying the outer membrane of Gram-negative bacteria is challenging due to the complex nature of its structure. Therefore, simplified models are required to undertake structure-function studies of processes that occur at the outer membrane/fluid interface. Model membranes can be created by immobilizing bilayers to solid supports such as gold or silicon surfaces, or as monolayers on a liquid support where the surface pressure and fluidity of the lipids can be controlled. Both model systems are amenable to having their structure probed by neutron reflectometry, a technique that provides a one-dimensional depth profile through a membrane detailing its thickness and composition. One of the strengths of neutron scattering is the ability to use contrast matching, allowing molecules containing hydrogen and those enriched with deuterium to be highlighted or matched out against the bulk isotopic composition of the solvent. Lipopolysaccharides, a major component of the outer membrane, can be isolated for incorporation into model membranes. Here, we describe the deuteration of lipopolysaccharides from rough strains of Escherichia coli for incorporation into model outer membranes, and how the use of deuterated materials enhances structural analysis of model membranes by neutron reflectometry.
Author(s): Le Brun AP, Clifton LA, Holt SA, Holden PJ, Lakey JH
Editor(s): Kumar CV
Publication type: Book Chapter
Publication status: Published
Book Title: Methods in Enzymology
Print publication date: 01/05/2017
Online publication date: 18/06/2015
Acceptance date: 01/01/1900
Publisher: Academic Press Inc.
Place Published: San Diego
Library holdings: Search Newcastle University Library for this item