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Issue 89, 2014
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New CHARMM force field parameters for dehydrated amino acid residues, the key to lantibiotic molecular dynamics simulations

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Abstract

Lantibiotics are an important class of naturally occurring antimicrobial peptides containing unusual dehydrated amino acid residues. In order to enable molecular dynamics simulations of lantibiotics, we have developed empirical force field parameters for dehydroalanine and dehydrobutyrine, which are compatible with the CHARMM all-atom force field. The parameters reproduce the geometries and energy barriers from MP2/6-31G*//MP2/cc-pVTZ quantum chemistry calculations. Experimental, predicted and calculated NMR chemical shifts for the amino protons and α-, β- and carbonyl carbon atoms of the dehydrated residues are consistent with a significant charge redistribution. The new parameters are used to perform the first molecular dynamics simulations of nisin, a widely used but poorly understood lantibiotic, in an aqueous environment and in a phospholipid bilayer. The simulations show surface association of the peptide with membranes in agreement with solid state NMR data and formation of β-turns in agreement with solution NMR.

Graphical abstract: New CHARMM force field parameters for dehydrated amino acid residues, the key to lantibiotic molecular dynamics simulations

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Publication details

The article was received on 05 Sep 2014, accepted on 22 Sep 2014 and first published on 22 Sep 2014


Article type: Paper
DOI: 10.1039/C4RA09897H
Citation: RSC Adv., 2014,4, 48621-48631
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    New CHARMM force field parameters for dehydrated amino acid residues, the key to lantibiotic molecular dynamics simulations

    E. R. Turpin, S. Mulholland, A. M. Teale, B. B. Bonev and J. D. Hirst, RSC Adv., 2014, 4, 48621
    DOI: 10.1039/C4RA09897H

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