Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.11851/1025
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dc.contributor.authorYazıcı, Hilal-
dc.contributor.authorO'Neill, Mary B.-
dc.contributor.authorKaçar, Turgay-
dc.contributor.authorWilson, Brandon R.-
dc.contributor.authorÖren, Ersin Emre-
dc.contributor.authorSarıkaya, Mehmet-
dc.contributor.authorTamerler, Candan-
dc.date.accessioned2019-05-23T05:48:44Z
dc.date.available2019-05-23T05:48:44Z
dc.date.issued2016-03
dc.identifier.citationYazici, H., O’Neill, M. B., Kacar, T., Wilson, B. R., Oren, E. E., Sarikaya, M., & Tamerler, C. (2016). Engineered chimeric peptides as antimicrobial surface coating agents toward infection-free implants. ACS applied materials & interfaces, 8(8), 5070-5081.en_US
dc.identifier.issn1944-8244
dc.identifier.othernumber of pages 12
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/acsami.5b03697-
dc.identifier.urihttps://hdl.handle.net/20.500.11851/1025-
dc.description.abstractPrevention of bacterial colonization and consequent biofilm formation remains a major challenge in implantable medical devices. Implant-associated infections are not only a major cause of implant failures but also their conventional treatment with antibiotics brings further complications due to the escalation in multidrug resistance to a variety of bacterial species. Owing to their unique properties, antimicrobial peptides (AMPs) have gained significant attention as effective agents to combat colonization of microorganisms. These peptides have been shown to exhibit a wide spectrum of activities with specificity to a target cell while having a low tendency for developing bacterial resistance. Engineering biomaterial surfaces that feature AMP properties, therefore, offer a promising approach to prevent implant infections. Here, we engineered a chimeric peptide with bifunctionality that both forms a robust solid-surface coating while presenting antimicrobial property. The individual domains of the chimeric peptides were evaluated for their solid-binding kinetics to titanium substrate as well as for their antimicrobial properties in solution. The antimicrobial efficacy of the chimeric peptide on the implant material was evaluated in vitro against infection by a variety of bacteria, including Streptococcus mutans, Staphylococcus. epidermidis, and Escherichia coli, which are commonly found in oral and orthopedic implant related surgeries. Our results demonstrate significant improvement in reducing bacterial colonization onto titanium surfaces below the detectable limit. Engineered chimeric peptides with freely displayed antimicrobial domains could be a potential solution for developing infection-free surfaces by engineering implant interfaces with highly reduced bacterial colonization property.en_US
dc.language.isoenen_US
dc.publisherAmer Chemical Socen_US
dc.relation.ispartofACS Applied Materials & Interfacesen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectmodular peptides and peptide-based implant coatingsen_US
dc.subjectinfectionen_US
dc.subjectsurface functionalizationen_US
dc.subjecttitanium binding peptides (tibp)en_US
dc.subjectantimicrobial peptide (amp)en_US
dc.subjectchimeric peptidesen_US
dc.titleEngineered Chimeric Peptides as Antimicrobial Surface Coating Agents toward Infection-Free Implantsen_US
dc.typeArticleen_US
dc.departmentFaculties, Faculty of Engineering, Department of Biomedical Engineeringen_US
dc.departmentFakülteler, Mühendislik Fakültesi, Biyomedikal Mühendisliği Bölümütr_TR
dc.identifier.volume8
dc.identifier.issue8
dc.identifier.startpage5070
dc.identifier.endpage5081
dc.authorid0000-0001-5902-083X-
dc.identifier.wosWOS:000371453600004en_US
dc.identifier.scopus2-s2.0-84959570442en_US
dc.institutionauthorÖren, Ersin Emre-
dc.identifier.pmid26795060en_US
dc.identifier.doi10.1021/acsami.5b03697-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.relation.otherNIH-NIAMS [AR062249-03]
dc.relation.otherNIH- NIDCR through University of Kansas and University of Washington [R01DE025476-01]
dc.relation.otherNSF-MRSEC Program through the University of Washington GEMSEC [DMR-0520567]
dc.identifier.scopusqualityQ1-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.languageiso639-1en-
crisitem.author.dept02.2. Department of Biomedical Engineering-
Appears in Collections:Biyomedikal Mühendisliği Bölümü / Department of Biomedical Engineering
PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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