Antibody purification from human plasma by metal-chelated affinity membranes
dc.authorid | 0000-0002-0920-2843 | en_US |
dc.authorid | 0000-0003-3260-1639 | |
dc.contributor.author | Yavuz, Handan | |
dc.contributor.author | Bereli, Nilay | |
dc.contributor.author | Armutçu, Canan | |
dc.contributor.author | Yılmaz, Fatma | |
dc.contributor.author | Denizli, Adil | |
dc.date.accessioned | 2021-06-23T19:28:46Z | |
dc.date.available | 2021-06-23T19:28:46Z | |
dc.date.issued | 2012 | |
dc.department | BAİBÜ, Gerede Meslek Yüksekokulu, Kimya Ve Kimyasal İşleme Teknolojileri Bölümü | en_US |
dc.description.abstract | The aim of this study is to investigate in detail the feasibility of poly(2-hydroxyethyl methacrylate-N-methacryloyl-(L)-histidine methyl ester), PHEMAH membranes for purification of immunoglobulin G (IgG) from human plasma. PHEMAH membranes were prepared by photo-polymerization technique. Then, Zn2+, Ni2+, Co2+, and Cu2+ ions were chelated directly on the PHEMAH membranes. Elemental analysis assay was performed to determine the nitrogen content and polymerized MAH was calculated as 168.5 mu mol/g. The nonspecific IgG adsorption onto the plain PHEMA membranes was negligible (about 0.25 mg/mL). A remarkable increase in the IgG adsorption capacities were achieved from human plasma with PHEMAH membranes (up to 68.4 mg/mL). Further increase was observed with the metal-chelated PHEMAH membranes (up to 118 mg/mL). The metal-chelate affinity membranes allowed the one-step separation of IgG from human plasma. The binding range of metal ions for surface histidines from human plasma followed the order: Cu2+ > Ni2+ > Zn2+ > Co2+. Adsorbed IgG was eluted using 250 mM EDTA with a purity of 94.1%. IgG molecules could be repeatedly adsorbed and eluted with the metal-chelated PHEMAH membranes without noticeable loss in their IgG adsorption capacity. (C) 2011 Wiley Periodicals, Inc. J Appl Polym Sci 123: 3476-3484, 2012 | en_US |
dc.identifier.doi | 10.1002/app.34672 | |
dc.identifier.endpage | 3484 | en_US |
dc.identifier.issn | 0021-8995 | |
dc.identifier.issn | 1097-4628 | |
dc.identifier.issue | 6 | en_US |
dc.identifier.scopus | 2-s2.0-82955203851 | en_US |
dc.identifier.scopusquality | Q2 | en_US |
dc.identifier.startpage | 3476 | en_US |
dc.identifier.uri | https://doi.org/10.1002/app.34672 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12491/7063 | |
dc.identifier.volume | 123 | en_US |
dc.identifier.wos | WOS:000298086500032 | en_US |
dc.identifier.wosquality | Q2 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.institutionauthor | Yılmaz, Fatma | |
dc.language.iso | en | en_US |
dc.publisher | Wiley | en_US |
dc.relation.ispartof | Journal Of Applied Polymer Science | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | IMAC | en_US |
dc.subject | Affinity Membranes | en_US |
dc.subject | Immunoglobulin-G | en_US |
dc.subject | PHEMA | en_US |
dc.title | Antibody purification from human plasma by metal-chelated affinity membranes | en_US |
dc.type | Article | en_US |
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