Molecularly imprinted nanoparticles with recognition properties towards diphtheria toxin for ELISA applications

dc.contributor.authorid0000-0003-4767-083X
dc.contributor.coauthorAlkanlı, Süleyman Serdar
dc.contributor.coauthorYaşar, Merve
dc.contributor.coauthorGüven, Celal
dc.contributor.coauthorKahraman, M. Vezir
dc.contributor.coauthorKayaman Apohan, Nilhan
dc.contributor.coauthorAktaş, Zerrin
dc.contributor.coauthorÖncül, Mustafa Oral
dc.contributor.coauthorÜnlü, Ayhan
dc.contributor.coauthorAkçakaya, Handan
dc.contributor.departmentN/A
dc.contributor.kuauthorYöntem, Fulya Dal
dc.contributor.kuprofileTeaching Faculty
dc.contributor.researchcenterKoç University Research Center for Translational Medicine (KUTTAM) / Koç Üniversitesi Translasyonel Tıp Araştırma Merkezi (KUTTAM)
dc.contributor.schoolcollegeinstituteSchool of Medicine
dc.contributor.unitKoç University Hospital
dc.contributor.yokid232576
dc.date.accessioned2025-01-19T10:30:08Z
dc.date.issued2023
dc.description.abstractPlastic antibodies can be used for in vitro neutralization of biomacromolecules with different fragments due to their potential in separation, purification, chemical sensor, catalysis and drug production studies. These polymer nanoparticles with binding affinity and selectivity comparable to natural antibodies were prepared using functional monomer synthesis and copolymerization of acrylic monomers via miniemulsion polymerization. As a result, the in vitro cytotoxic effect from diphtheria toxin was reduced by MIPs. In vitro imaging experiments of polymer nanoparticles (plastic antibodies) were performed to examine the interaction of diphtheria toxin with actin filaments, and MIPs inhibited diphtheria toxin damage on actin filaments. The enzyme-linked immunosorbent assay (ELISA) was performed with plastic antibodies labeled with biotin, and it was determined that plastic antibodies could also be used for diagnostic purposes. We report that molecularly imprinted polymers (MIPs), which are biocompatible polymer nanoparticles, can capture and reduce the effect of diphtheria toxic and its fragment A.
dc.description.indexedbyWoS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue6
dc.description.publisherscopeInternational
dc.description.sponsorsFinancial assistance for this research by The Scientific and Technological Research Council of Turkey (TUBITAK Project No. 115S224); and The Scientific Research Projects Coordination Unit of Istanbul University (BAP Project No. 25648).
dc.description.volume34
dc.identifier.doi10.1080/09205063.2022.2145866
dc.identifier.issn0920-5063
dc.identifier.quartileQ2
dc.identifier.scopus2-s2.0-85142129163
dc.identifier.urihttps://doi.org/10.1080/09205063.2022.2145866
dc.identifier.urihttps://hdl.handle.net/20.500.14288/25985
dc.identifier.wos889094600001
dc.keywordsDiphtheria toxin
dc.keywordsELISA
dc.keywordsMolecularly imprinted polymer
dc.keywordsPlastic antibody
dc.languageen
dc.publisherTaylor and Francis Ltd.
dc.relation.grantnoIstanbul Üniversitesi; Türkiye Bilimsel ve Teknolojik Araştırma Kurumu, TÜBİTAK, (115S224); Bilimsel Araştırma Projeleri Birimi, İstanbul Teknik Üniversitesi, BAP, (25648)
dc.sourceJournal of Biomaterials Science, Polymer Edition
dc.subjectEngineering, biomedical
dc.subjectMaterials science
dc.subjectBiomaterials
dc.subjectPolymer science
dc.titleMolecularly imprinted nanoparticles with recognition properties towards diphtheria toxin for ELISA applications
dc.typeJournal Article

Files