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Exploring the links between peptoid antibacterial activity and toxicity
Peptoids are a promising class of antimicrobial agents with reported activities against a range of both Gram-positive and Gram-negative bacteria, fungi and most recently parasites. However, at present the available toxicity data is somewhat limited and as such rationally designing effective antimicr...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6072100/ https://www.ncbi.nlm.nih.gov/pubmed/30108804 http://dx.doi.org/10.1039/c6md00648e |
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author | Bolt, H. L. Eggimann, G. A. Jahoda, C. A. B. Zuckermann, R. N. Sharples, G. J. Cobb, S. L. |
author_facet | Bolt, H. L. Eggimann, G. A. Jahoda, C. A. B. Zuckermann, R. N. Sharples, G. J. Cobb, S. L. |
author_sort | Bolt, H. L. |
collection | PubMed |
description | Peptoids are a promising class of antimicrobial agents with reported activities against a range of both Gram-positive and Gram-negative bacteria, fungi and most recently parasites. However, at present the available toxicity data is somewhat limited and as such rationally designing effective antimicrobial peptoids can be challenging. Herein, we present the toxicity profiling of a series of linear peptoids against mammalian cell lines (HaCaT and HepG2). The cytotoxicity of the peptoid library has then been correlated with their antibacterial properties against Gram-positive and Gram-negative bacteria and also to the hydrophobicity of the peptoid sequences. The work presented provides valuable data to aid in the future rational design of antimicrobial peptoids. |
format | Online Article Text |
id | pubmed-6072100 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-60721002018-08-14 Exploring the links between peptoid antibacterial activity and toxicity Bolt, H. L. Eggimann, G. A. Jahoda, C. A. B. Zuckermann, R. N. Sharples, G. J. Cobb, S. L. Medchemcomm Chemistry Peptoids are a promising class of antimicrobial agents with reported activities against a range of both Gram-positive and Gram-negative bacteria, fungi and most recently parasites. However, at present the available toxicity data is somewhat limited and as such rationally designing effective antimicrobial peptoids can be challenging. Herein, we present the toxicity profiling of a series of linear peptoids against mammalian cell lines (HaCaT and HepG2). The cytotoxicity of the peptoid library has then been correlated with their antibacterial properties against Gram-positive and Gram-negative bacteria and also to the hydrophobicity of the peptoid sequences. The work presented provides valuable data to aid in the future rational design of antimicrobial peptoids. Royal Society of Chemistry 2017-02-01 /pmc/articles/PMC6072100/ /pubmed/30108804 http://dx.doi.org/10.1039/c6md00648e Text en This journal is © The Royal Society of Chemistry 2017 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0) |
spellingShingle | Chemistry Bolt, H. L. Eggimann, G. A. Jahoda, C. A. B. Zuckermann, R. N. Sharples, G. J. Cobb, S. L. Exploring the links between peptoid antibacterial activity and toxicity |
title | Exploring the links between peptoid antibacterial activity and toxicity
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title_full | Exploring the links between peptoid antibacterial activity and toxicity
|
title_fullStr | Exploring the links between peptoid antibacterial activity and toxicity
|
title_full_unstemmed | Exploring the links between peptoid antibacterial activity and toxicity
|
title_short | Exploring the links between peptoid antibacterial activity and toxicity
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title_sort | exploring the links between peptoid antibacterial activity and toxicity |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6072100/ https://www.ncbi.nlm.nih.gov/pubmed/30108804 http://dx.doi.org/10.1039/c6md00648e |
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