Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/106661
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Type: Journal article
Title: Determining the structure of interfacial peptide films: comparing neutron reflectometry and molecular dynamics simulations
Author: Xue, Y.
He, L.
Middelberg, A.
Mark, A.
Poger, D.
Citation: Langmuir: the ACS journal of surfaces and colloids, 2014; 30(33):10080-10089
Publisher: American Chemical Society
Issue Date: 2014
ISSN: 0743-7463
1520-5827
Statement of
Responsibility: 
Ying Xue, Lizhong He, Anton P. J. Middelberg, Alan E. Mark, and David Poger
Abstract: The peptides AM1 and Lac21E self-organize into switchable films at an air-water interface. In an earlier study, it was proposed that both AM1 and Lac21E formed monolayers of α-helical peptides based on consistency with neutron reflectivity data. In this article, molecular dynamics simulations of assemblies of helical and nonhelical AM1 and Lac21E at an air-water interface suggest some tendency for the peptides to spontaneously adopt an α-helical conformation. However, irrespective of the structure of the peptides, the simulations reproduced not only the structural properties of the films (thickness and distribution of the hydrophobic and hydrophilic amino acids) but also the experimental neutron reflectivity measurements at different contrast variations. This suggests that neutron reflectometry alone cannot be used to determine the structure of the peptides in this case. However, together with molecular dynamics simulations, it is possible to obtain a detailed understanding of peptide films at an atomic level.
Keywords: Peptides
Description: Published: August 5, 2014
Rights: © 2014 American Chemical Society
DOI: 10.1021/la501715h
Grant ID: http://purl.org/au-research/grants/arc/DP110100327
http://purl.org/au-research/grants/arc/DP130102153
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Chemical Engineering publications

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