A Novel Route To Prepare a Multilayer System Via the Combination of Interface-Mediated Catalytic Chain Transfer Polymerization and Thiol-Ene Click Chemistry
dc.authorscopusid | 36718519300 | |
dc.authorscopusid | 7004083315 | |
dc.contributor.author | Zengin, Adem | |
dc.contributor.author | Caykara, Tuncer | |
dc.date.accessioned | 2025-05-10T17:28:04Z | |
dc.date.available | 2025-05-10T17:28:04Z | |
dc.date.issued | 2017 | |
dc.department | T.C. Van Yüzüncü Yıl Üniversitesi | en_US |
dc.department-temp | [Zengin, Adem] Yuzuncu Yil Univ, Fac Engn & Architecture, Dept Chem Engn, TR-65080 Van, Turkey; [Caykara, Tuncer] Gazi Univ, Fac Sci, Dept Chem, TR-06500 Ankara, Turkey | en_US |
dc.description.abstract | Herein, we have designed a novel multilayer system composed of poly(methyl methacrylate) [poly(MMA)] brush, biotin, streptavidin and protein-A on a silicon substrate to attach on anti-immunoglobulin G (anti-IgG). poly(MMA) brush with vinyl end-group was first synthesized by the interface-mediated catalytic chain transfer polymerization. The brush was then modified with cysteamine molecules to generate the polymer chains with amine end-group via a thiol-ene click chemistry. The amine end-groups of poly(MMA) chains were also modified with biotin units to ensure selective connection points for streptavidin molecules. Finally, a multilayer system on the silicon substrate was formed by using streptavidin and protein-A molecules, respectively. This multilayer system was employed to attach anti-IgG molecules in a highly oriented manner and provide anti-IgG molecular functional configuration on the multilayer. High reproducibility of the amount of anti-IgG adsorption and homogeneous anti-IgG adsorption layer on the silicon surface could be provided by this multilayer system. The multi layer system with protein A may be opened the door for designing an efficient immunoassay protein chip. (C) 2017 Published by Elsevier B.V. | en_US |
dc.description.woscitationindex | Science Citation Index Expanded | |
dc.identifier.doi | 10.1016/j.msec.2017.02.011 | |
dc.identifier.endpage | 109 | en_US |
dc.identifier.issn | 0928-4931 | |
dc.identifier.issn | 1873-0191 | |
dc.identifier.pmid | 28254273 | |
dc.identifier.scopus | 2-s2.0-85011976014 | |
dc.identifier.scopusquality | N/A | |
dc.identifier.startpage | 103 | en_US |
dc.identifier.uri | https://doi.org/10.1016/j.msec.2017.02.011 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14720/11936 | |
dc.identifier.volume | 74 | en_US |
dc.identifier.wos | WOS:000397356900012 | |
dc.identifier.wosquality | N/A | |
dc.language.iso | en | en_US |
dc.publisher | Elsevier | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Surface-Mediated Catalytic Chain Transfer Polymerization | en_US |
dc.subject | Thiol-Ene Click Chemistry | en_US |
dc.subject | Poly(Methyl Methacrylate) Brushes | en_US |
dc.subject | Anti-Immunoglobulin G | en_US |
dc.title | A Novel Route To Prepare a Multilayer System Via the Combination of Interface-Mediated Catalytic Chain Transfer Polymerization and Thiol-Ene Click Chemistry | en_US |
dc.type | Article | en_US |