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Broad-Spectrum Antimicrobial Activity and Improved Stability of a D-Amino Acid Enantiomer of DMPC-10A, the Designed Derivative of Dermaseptin Truncates
DMPC-10A (ALWKKLLKK-Cha-NH(2)) is a 10-mer peptide derivative from the N-terminal domain of Dermaseptin-PC which has shown broad-spectrum antimicrobial activity as well as a considerable hemolytic effect. In order to reduce hemolytic activity and improve stability to endogenous enzymes, a D-amino ac...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7557582/ https://www.ncbi.nlm.nih.gov/pubmed/32967333 http://dx.doi.org/10.3390/antibiotics9090627 |
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author | Zai, Yu Ying, Yuan Ye, Zhuming Zhou, Mei Ma, Chengbang Shi, Zhanzhong Chen, Xiaoling Xi, Xinping Chen, Tianbao Wang, Lei |
author_facet | Zai, Yu Ying, Yuan Ye, Zhuming Zhou, Mei Ma, Chengbang Shi, Zhanzhong Chen, Xiaoling Xi, Xinping Chen, Tianbao Wang, Lei |
author_sort | Zai, Yu |
collection | PubMed |
description | DMPC-10A (ALWKKLLKK-Cha-NH(2)) is a 10-mer peptide derivative from the N-terminal domain of Dermaseptin-PC which has shown broad-spectrum antimicrobial activity as well as a considerable hemolytic effect. In order to reduce hemolytic activity and improve stability to endogenous enzymes, a D-amino acid enantiomer (DMPC-10B) was designed by substituting all L-Lys and L-Leu with their respective D-form amino acid residues, while the Ala(1) and Trp(3) remained unchanged. The D-amino acid enantiomer exhibited similar antimicrobial potency to the parent peptide but exerted lower cytotoxicity and hemolytic activity. Meanwhile, DMPC-10B exhibited remarkable resistance to hydrolysis by trypsin and chymotrypsin. In addition to these advantages, DMPC-10B exhibited an outstanding antibacterial effect against Methicillin-resistant Staphylococcus aureus (MRSA) and Klebsiella pneumoniae using the Galleria mellonella larva model and displayed synergistic activities with gentamicin against carbapenem-resistant K. pneumoniae strains. This indicates that DMPC-10B would be a promising alternative for treating antibiotic-resistant pathogens. |
format | Online Article Text |
id | pubmed-7557582 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-75575822020-10-20 Broad-Spectrum Antimicrobial Activity and Improved Stability of a D-Amino Acid Enantiomer of DMPC-10A, the Designed Derivative of Dermaseptin Truncates Zai, Yu Ying, Yuan Ye, Zhuming Zhou, Mei Ma, Chengbang Shi, Zhanzhong Chen, Xiaoling Xi, Xinping Chen, Tianbao Wang, Lei Antibiotics (Basel) Article DMPC-10A (ALWKKLLKK-Cha-NH(2)) is a 10-mer peptide derivative from the N-terminal domain of Dermaseptin-PC which has shown broad-spectrum antimicrobial activity as well as a considerable hemolytic effect. In order to reduce hemolytic activity and improve stability to endogenous enzymes, a D-amino acid enantiomer (DMPC-10B) was designed by substituting all L-Lys and L-Leu with their respective D-form amino acid residues, while the Ala(1) and Trp(3) remained unchanged. The D-amino acid enantiomer exhibited similar antimicrobial potency to the parent peptide but exerted lower cytotoxicity and hemolytic activity. Meanwhile, DMPC-10B exhibited remarkable resistance to hydrolysis by trypsin and chymotrypsin. In addition to these advantages, DMPC-10B exhibited an outstanding antibacterial effect against Methicillin-resistant Staphylococcus aureus (MRSA) and Klebsiella pneumoniae using the Galleria mellonella larva model and displayed synergistic activities with gentamicin against carbapenem-resistant K. pneumoniae strains. This indicates that DMPC-10B would be a promising alternative for treating antibiotic-resistant pathogens. MDPI 2020-09-21 /pmc/articles/PMC7557582/ /pubmed/32967333 http://dx.doi.org/10.3390/antibiotics9090627 Text en © 2020 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 | Article Zai, Yu Ying, Yuan Ye, Zhuming Zhou, Mei Ma, Chengbang Shi, Zhanzhong Chen, Xiaoling Xi, Xinping Chen, Tianbao Wang, Lei Broad-Spectrum Antimicrobial Activity and Improved Stability of a D-Amino Acid Enantiomer of DMPC-10A, the Designed Derivative of Dermaseptin Truncates |
title | Broad-Spectrum Antimicrobial Activity and Improved Stability of a D-Amino Acid Enantiomer of DMPC-10A, the Designed Derivative of Dermaseptin Truncates |
title_full | Broad-Spectrum Antimicrobial Activity and Improved Stability of a D-Amino Acid Enantiomer of DMPC-10A, the Designed Derivative of Dermaseptin Truncates |
title_fullStr | Broad-Spectrum Antimicrobial Activity and Improved Stability of a D-Amino Acid Enantiomer of DMPC-10A, the Designed Derivative of Dermaseptin Truncates |
title_full_unstemmed | Broad-Spectrum Antimicrobial Activity and Improved Stability of a D-Amino Acid Enantiomer of DMPC-10A, the Designed Derivative of Dermaseptin Truncates |
title_short | Broad-Spectrum Antimicrobial Activity and Improved Stability of a D-Amino Acid Enantiomer of DMPC-10A, the Designed Derivative of Dermaseptin Truncates |
title_sort | broad-spectrum antimicrobial activity and improved stability of a d-amino acid enantiomer of dmpc-10a, the designed derivative of dermaseptin truncates |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7557582/ https://www.ncbi.nlm.nih.gov/pubmed/32967333 http://dx.doi.org/10.3390/antibiotics9090627 |
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