Surface Triggered Self-Assembly of Fmoc-Tripeptide as an Antibacterial Coating
In western countries, one patient on twenty will develop a nosocomial infection during his hospitalization at health care facilities. Classical antibiotics being less and less effective, this phenomenon is expanding year after year. Prevention of bacteria colonization of implantable medical devices...
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doaj-8a694672e67847208a05903fe28b38062020-11-25T03:11:30ZengFrontiers Media S.A.Frontiers in Bioengineering and Biotechnology2296-41852020-08-01810.3389/fbioe.2020.00938561821Surface Triggered Self-Assembly of Fmoc-Tripeptide as an Antibacterial CoatingMiryam Criado-Gonzalez0Miryam Criado-Gonzalez1Muhammad Haseeb Iqbal2Muhammad Haseeb Iqbal3Alain Carvalho4Marc Schmutz5Loïc Jierry6Pierre Schaaf7Pierre Schaaf8Pierre Schaaf9Fouzia Boulmedais10Université de Strasbourg, CNRS, Institut Charles Sadron UPR 22, Strasbourg, FranceInstitut National de la Santé et de la Recherche Médicale, UMR-S 1121, “Biomatériaux et Bioingénierie”, Strasbourg, FranceUniversité de Strasbourg, CNRS, Institut Charles Sadron UPR 22, Strasbourg, FranceInstitut National de la Santé et de la Recherche Médicale, UMR-S 1121, “Biomatériaux et Bioingénierie”, Strasbourg, FranceUniversité de Strasbourg, CNRS, Institut Charles Sadron UPR 22, Strasbourg, FranceUniversité de Strasbourg, CNRS, Institut Charles Sadron UPR 22, Strasbourg, FranceUniversité de Strasbourg, CNRS, Institut Charles Sadron UPR 22, Strasbourg, FranceUniversité de Strasbourg, CNRS, Institut Charles Sadron UPR 22, Strasbourg, FranceInstitut National de la Santé et de la Recherche Médicale, UMR-S 1121, “Biomatériaux et Bioingénierie”, Strasbourg, FranceFaculté de Chirurgie Dentaire, Fédération de Médecine Translationnelle de Strasbourg and Fédération des Matériaux et Nanoscience d’Alsace, Université de Strasbourg, Strasbourg, FranceUniversité de Strasbourg, CNRS, Institut Charles Sadron UPR 22, Strasbourg, FranceIn western countries, one patient on twenty will develop a nosocomial infection during his hospitalization at health care facilities. Classical antibiotics being less and less effective, this phenomenon is expanding year after year. Prevention of bacteria colonization of implantable medical devices constitutes a major medical and financial issue. In this study, we developed an antibacterial coating based on self-assembled Fmoc-tripeptide. Fmoc-FFpY peptides (F: phenylalanine; Y: tyrosine; p: PO42–) are dephosphorylated enzymatically into Fmoc-FFY by action of alkaline phosphatase functionalized silica nanoparticles (NPs@AP), previously deposited on a surface. Fmoc-FFY peptides then self-assemble through π–π stacking interactions, hydrogen bonds and hydrophobic interactions adopting β-sheets secondary structures. The obtained hydrogel coatings show fibrillary structures observed by cryo-scanning electron microscopy with a thickness of few micrometers. At low concentration (≤0.5 mg.mL–1), self-assembled Fmoc-FFY has a superior antibacterial activity than Fmoc-FFpY peptide in solution. After 24 h of incubation, Fmoc-FFY hydrogel coatings fully inhibit the development of Gram-positive Staphylococcus aureus (S. aureus). The antibacterial effect is maintained on an in vitro model of repetitive infection in the case of S. aureus. This coating could serve in infections were Gram positive bacteria are prevalent, e.g., intravascular catheter infections. This work gives new insights toward the design of an alternative antimicrobial coating.https://www.frontiersin.org/article/10.3389/fbioe.2020.00938/fullpeptideshydrogelsantimicrobialenzyme-assisted self-assemblynanoparticles |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Miryam Criado-Gonzalez Miryam Criado-Gonzalez Muhammad Haseeb Iqbal Muhammad Haseeb Iqbal Alain Carvalho Marc Schmutz Loïc Jierry Pierre Schaaf Pierre Schaaf Pierre Schaaf Fouzia Boulmedais |
spellingShingle |
Miryam Criado-Gonzalez Miryam Criado-Gonzalez Muhammad Haseeb Iqbal Muhammad Haseeb Iqbal Alain Carvalho Marc Schmutz Loïc Jierry Pierre Schaaf Pierre Schaaf Pierre Schaaf Fouzia Boulmedais Surface Triggered Self-Assembly of Fmoc-Tripeptide as an Antibacterial Coating Frontiers in Bioengineering and Biotechnology peptides hydrogels antimicrobial enzyme-assisted self-assembly nanoparticles |
author_facet |
Miryam Criado-Gonzalez Miryam Criado-Gonzalez Muhammad Haseeb Iqbal Muhammad Haseeb Iqbal Alain Carvalho Marc Schmutz Loïc Jierry Pierre Schaaf Pierre Schaaf Pierre Schaaf Fouzia Boulmedais |
author_sort |
Miryam Criado-Gonzalez |
title |
Surface Triggered Self-Assembly of Fmoc-Tripeptide as an Antibacterial Coating |
title_short |
Surface Triggered Self-Assembly of Fmoc-Tripeptide as an Antibacterial Coating |
title_full |
Surface Triggered Self-Assembly of Fmoc-Tripeptide as an Antibacterial Coating |
title_fullStr |
Surface Triggered Self-Assembly of Fmoc-Tripeptide as an Antibacterial Coating |
title_full_unstemmed |
Surface Triggered Self-Assembly of Fmoc-Tripeptide as an Antibacterial Coating |
title_sort |
surface triggered self-assembly of fmoc-tripeptide as an antibacterial coating |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Bioengineering and Biotechnology |
issn |
2296-4185 |
publishDate |
2020-08-01 |
description |
In western countries, one patient on twenty will develop a nosocomial infection during his hospitalization at health care facilities. Classical antibiotics being less and less effective, this phenomenon is expanding year after year. Prevention of bacteria colonization of implantable medical devices constitutes a major medical and financial issue. In this study, we developed an antibacterial coating based on self-assembled Fmoc-tripeptide. Fmoc-FFpY peptides (F: phenylalanine; Y: tyrosine; p: PO42–) are dephosphorylated enzymatically into Fmoc-FFY by action of alkaline phosphatase functionalized silica nanoparticles (NPs@AP), previously deposited on a surface. Fmoc-FFY peptides then self-assemble through π–π stacking interactions, hydrogen bonds and hydrophobic interactions adopting β-sheets secondary structures. The obtained hydrogel coatings show fibrillary structures observed by cryo-scanning electron microscopy with a thickness of few micrometers. At low concentration (≤0.5 mg.mL–1), self-assembled Fmoc-FFY has a superior antibacterial activity than Fmoc-FFpY peptide in solution. After 24 h of incubation, Fmoc-FFY hydrogel coatings fully inhibit the development of Gram-positive Staphylococcus aureus (S. aureus). The antibacterial effect is maintained on an in vitro model of repetitive infection in the case of S. aureus. This coating could serve in infections were Gram positive bacteria are prevalent, e.g., intravascular catheter infections. This work gives new insights toward the design of an alternative antimicrobial coating. |
topic |
peptides hydrogels antimicrobial enzyme-assisted self-assembly nanoparticles |
url |
https://www.frontiersin.org/article/10.3389/fbioe.2020.00938/full |
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