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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Main Authors: Miryam Criado-Gonzalez, Muhammad Haseeb Iqbal, Alain Carvalho, Marc Schmutz, Loïc Jierry, Pierre Schaaf, Fouzia Boulmedais
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-08-01
Series:Frontiers in Bioengineering and Biotechnology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fbioe.2020.00938/full
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spelling 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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