Nontoxic antimicrobial cationic peptide nanoconstructs with bacteria-displaceable polymeric counteranions
Antimicrobial peptides that target the integrity of bacterial envelopes can eradicate pathogens with little development of resistance, but they often inflict nonselective toxicity toward mammalian cells. The prevailing approach to optimize the selectivity of cationic peptides has been to modify thei...
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sg-ntu-dr.10356-1540402023-02-28T19:59:44Z Nontoxic antimicrobial cationic peptide nanoconstructs with bacteria-displaceable polymeric counteranions Pranantyo, Dicky Raju, Cheerlavancha Si, Zhangyong Xu, Xiaofei Pethe, Kevin Kang, En-Tang Chan-Park, Mary B. School of Chemical and Biomedical Engineering School of Physical and Mathematical Sciences Lee Kong Chian School of Medicine (LKCMedicine) Centre for Antimicrobial Bioengineering Engineering::Chemical engineering::Polymers and polymer manufacture Electrostatic Nanoconstructs Competitive Displacement Antimicrobial peptides that target the integrity of bacterial envelopes can eradicate pathogens with little development of resistance, but they often inflict nonselective toxicity toward mammalian cells. The prevailing approach to optimize the selectivity of cationic peptides has been to modify their composition. Instead, we invent a new generation of broad-spectrum antibacterial nanoconstructs with negligible mammalian cell toxicity through a competitive displacement of counter polyanions from the complementary polycations. The nanoconstruct, which has a highly cationic Au nanoparticles (NPs) core shielded by polymeric counterions, is inert in nonbacterial environments. When exposed to negatively charged bacterial envelopes, this construct sheds its polyanions, triggering a cationic Au NP/bacterial membrane interaction that rapidly kills Gram-positive and Gram-negative bacteria. The anionic charge and hydrophilicity of the polyanion provides charge neutralization for the peptide-decorated Au NP core, but it is also bacteria-displaceable. These results provide a foundation for the development of other cationic particles and polymeric counterion combinations with potent antimicrobial activity without toxicity. Agency for Science, Technology and Research (A*STAR) Ministry of Education (MOE) Nanyang Technological University Accepted version This work was funded and supported by the Singapore Ministry of Education Tier 3 Grants (MOE2013-T3-1-002 and MOE2018-T3-1-003), ASTAR RIE2020 Advanced Manufacturing and Engineering (AME) IAP-PP Specialty Chemicals Programme Grant (No. A1786a0032), and NTU NAFTEC Funding. 2021-12-15T02:38:09Z 2021-12-15T02:38:09Z 2021 Journal Article Pranantyo, D., Raju, C., Si, Z., Xu, X., Pethe, K., Kang, E. & Chan-Park, M. B. (2021). Nontoxic antimicrobial cationic peptide nanoconstructs with bacteria-displaceable polymeric counteranions. Nano Letters, 21(2), 899-906. https://dx.doi.org/10.1021/acs.nanolett.0c03261 1530-6984 https://hdl.handle.net/10356/154040 10.1021/acs.nanolett.0c03261 2 21 899 906 en MOE2013-T3-1-002 MOE2018-T3-1-003 A1786a0032 Nano Letters This document is the Accepted Manuscript version of a Published Work that appeared in final form in Nano Letters, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.nanolett.0c03261. application/pdf |
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Engineering::Chemical engineering::Polymers and polymer manufacture Electrostatic Nanoconstructs Competitive Displacement Pranantyo, Dicky Raju, Cheerlavancha Si, Zhangyong Xu, Xiaofei Pethe, Kevin Kang, En-Tang Chan-Park, Mary B. Nontoxic antimicrobial cationic peptide nanoconstructs with bacteria-displaceable polymeric counteranions |
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Antimicrobial peptides that target the integrity of bacterial envelopes can eradicate pathogens with little development of resistance, but they often inflict nonselective toxicity toward mammalian cells. The prevailing approach to optimize the selectivity of cationic peptides has been to modify their composition. Instead, we invent a new generation of broad-spectrum antibacterial nanoconstructs with negligible mammalian cell toxicity through a competitive displacement of counter polyanions from the complementary polycations. The nanoconstruct, which has a highly cationic Au nanoparticles (NPs) core shielded by polymeric counterions, is inert in nonbacterial environments. When exposed to negatively charged bacterial envelopes, this construct sheds its polyanions, triggering a cationic Au NP/bacterial membrane interaction that rapidly kills Gram-positive and Gram-negative bacteria. The anionic charge and hydrophilicity of the polyanion provides charge neutralization for the peptide-decorated Au NP core, but it is also bacteria-displaceable. These results provide a foundation for the development of other cationic particles and polymeric counterion combinations with potent antimicrobial activity without toxicity. |
author2 |
School of Chemical and Biomedical Engineering |
author_facet |
School of Chemical and Biomedical Engineering Pranantyo, Dicky Raju, Cheerlavancha Si, Zhangyong Xu, Xiaofei Pethe, Kevin Kang, En-Tang Chan-Park, Mary B. |
format |
Article |
author |
Pranantyo, Dicky Raju, Cheerlavancha Si, Zhangyong Xu, Xiaofei Pethe, Kevin Kang, En-Tang Chan-Park, Mary B. |
author_sort |
Pranantyo, Dicky |
title |
Nontoxic antimicrobial cationic peptide nanoconstructs with bacteria-displaceable polymeric counteranions |
title_short |
Nontoxic antimicrobial cationic peptide nanoconstructs with bacteria-displaceable polymeric counteranions |
title_full |
Nontoxic antimicrobial cationic peptide nanoconstructs with bacteria-displaceable polymeric counteranions |
title_fullStr |
Nontoxic antimicrobial cationic peptide nanoconstructs with bacteria-displaceable polymeric counteranions |
title_full_unstemmed |
Nontoxic antimicrobial cationic peptide nanoconstructs with bacteria-displaceable polymeric counteranions |
title_sort |
nontoxic antimicrobial cationic peptide nanoconstructs with bacteria-displaceable polymeric counteranions |
publishDate |
2021 |
url |
https://hdl.handle.net/10356/154040 |
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1759857232649912320 |