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Investigation of the N-Terminus Amino Function of Arg(10)-Teixobactin

Teixobactin is a recently described antimicrobial peptide that shows high activity against gram-positive bacteria as well as mycobacterium tuberculosis. Due to both its structure as a head-to-side chain cyclodepsipeptide and its activity, it has attracted the attention of several research groups. In...

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Autores principales: Abdel Monaim, Shimaa A. H., Noki, Sikabwe, Ramchuran, Estelle J., El-Faham, Ayman, Albericio, Fernando, de la Torre, Beatriz G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151525/
https://www.ncbi.nlm.nih.gov/pubmed/28956840
http://dx.doi.org/10.3390/molecules22101632
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author Abdel Monaim, Shimaa A. H.
Noki, Sikabwe
Ramchuran, Estelle J.
El-Faham, Ayman
Albericio, Fernando
de la Torre, Beatriz G.
author_facet Abdel Monaim, Shimaa A. H.
Noki, Sikabwe
Ramchuran, Estelle J.
El-Faham, Ayman
Albericio, Fernando
de la Torre, Beatriz G.
author_sort Abdel Monaim, Shimaa A. H.
collection PubMed
description Teixobactin is a recently described antimicrobial peptide that shows high activity against gram-positive bacteria as well as mycobacterium tuberculosis. Due to both its structure as a head-to-side chain cyclodepsipeptide and its activity, it has attracted the attention of several research groups. In this regard, a large number of analogs with substitutions in both the cycle and the tail has been described. Here, we report the contribution of the N-terminus residue, N-Me-d-Phe, to the activity of Arg(10)-teixobactin. On the basis of our findings, we conclude that the N-terminus accepts minimum changes but not the presence of long alkyl chains. The presence of a positive charge is a requirement for the activity of the peptide. Furthermore, acylation of the N-terminus leads to total loss of activity.
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spelling pubmed-61515252018-11-13 Investigation of the N-Terminus Amino Function of Arg(10)-Teixobactin Abdel Monaim, Shimaa A. H. Noki, Sikabwe Ramchuran, Estelle J. El-Faham, Ayman Albericio, Fernando de la Torre, Beatriz G. Molecules Communication Teixobactin is a recently described antimicrobial peptide that shows high activity against gram-positive bacteria as well as mycobacterium tuberculosis. Due to both its structure as a head-to-side chain cyclodepsipeptide and its activity, it has attracted the attention of several research groups. In this regard, a large number of analogs with substitutions in both the cycle and the tail has been described. Here, we report the contribution of the N-terminus residue, N-Me-d-Phe, to the activity of Arg(10)-teixobactin. On the basis of our findings, we conclude that the N-terminus accepts minimum changes but not the presence of long alkyl chains. The presence of a positive charge is a requirement for the activity of the peptide. Furthermore, acylation of the N-terminus leads to total loss of activity. MDPI 2017-09-28 /pmc/articles/PMC6151525/ /pubmed/28956840 http://dx.doi.org/10.3390/molecules22101632 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Abdel Monaim, Shimaa A. H.
Noki, Sikabwe
Ramchuran, Estelle J.
El-Faham, Ayman
Albericio, Fernando
de la Torre, Beatriz G.
Investigation of the N-Terminus Amino Function of Arg(10)-Teixobactin
title Investigation of the N-Terminus Amino Function of Arg(10)-Teixobactin
title_full Investigation of the N-Terminus Amino Function of Arg(10)-Teixobactin
title_fullStr Investigation of the N-Terminus Amino Function of Arg(10)-Teixobactin
title_full_unstemmed Investigation of the N-Terminus Amino Function of Arg(10)-Teixobactin
title_short Investigation of the N-Terminus Amino Function of Arg(10)-Teixobactin
title_sort investigation of the n-terminus amino function of arg(10)-teixobactin
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151525/
https://www.ncbi.nlm.nih.gov/pubmed/28956840
http://dx.doi.org/10.3390/molecules22101632
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