Ti (IV) attached-phosphonic acid functionalized capillary monolith as a stationary phase for in-syringe-type fast and robust enrichment of phosphopeptides

dc.authorid0000-0002-9353-7880
dc.contributor.authorSalimi, Kouroush
dc.contributor.authorKip, Cigdem
dc.contributor.authorCelikbicak, Omur
dc.contributor.authorUsta, Duygu Deniz
dc.contributor.authorPinar, Asli
dc.contributor.authorSalih, Bekir
dc.contributor.authorTuncel, Ali
dc.date.accessioned2025-05-10T19:53:35Z
dc.date.issued2019
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractIn this study, poly(vinylphosphonic acid-co-ethylene dimethacrylate), poly(VPA-co-EDMA) capillary monolith was synthesized as a starting material for obtaining a stationary phase for microscale enrichment of phosphopeptides. The chelation of active phosphonate groups with Ti (IV) ions gave a macroporous monolithic column with a mean pore size of 5.4 mu m. The phosphopeptides from different sources were enriched on Ti (IV)-attached poly(VPA-co-EDMA) monolith using a syringe-pump. The monolithic capillary columns exhibited highly sensitive/selective enrichment performance with phosphoprotein concentrations as low as 1.0 fmol/mL. Six different phosphopeptides were detected with high intensity by the treatment of beta-casein digest with the concentration of 1.0 fmol/mL, using Ti (IV)@poly(VPA-co-EDMA) monolith. Highly selective enrichment of phosphopeptides was also successfully carried out even at trace amounts, in a complex mixture of digested proteins (molar ratio of beta-casein to bovine serum albumin, 1:1500) and three phosphopeptides were successfully detected. Four highly intense signals of phosphopeptides in human serum were also observed with high signal-to-noise ratio and a clear background after enrichment with Ti (IV)@poly(VPA-co-EDMA) monolith. It was concluded that the capillary microextraction system enabled fast, efficient and robust enrichment of phosphopeptides from microscale complex samples. The whole enrichment process was completed within 20 min, which was shorter than in the previously reported studies.
dc.description.sponsorshipTurkiye Bilimler Akademisi; Turkiye Bilimsel ve Teknolojik Arastirma Kurumu [2211-E]; TUBITAK, BIDEB [2211-E]; Turkish Academy of Sciences
dc.description.sponsorshipTurkiye Bilimler Akademisi; Turkiye Bilimsel ve Teknolojik Arastirma Kurumu, Grant/Award Number: 2211-E; TUBITAK, BIDEB, Grant/Award Number: 2211-E; Turkish Academy of Sciences
dc.identifier.doi10.1002/bmc.4488
dc.identifier.issn0269-3879
dc.identifier.issn1099-0801
dc.identifier.issue6
dc.identifier.pmid30656732
dc.identifier.scopus2-s2.0-85061034949
dc.identifier.scopusqualityQ3
dc.identifier.urihttps://doi.org/10.1002/bmc.4488
dc.identifier.urihttps://hdl.handle.net/20.500.14730/12779
dc.identifier.volume33
dc.identifier.wosWOS:000467860100011
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherWiley
dc.relation.ispartofBiomedical Chromatography
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WOS_20250302
dc.subjectcapillary monolith
dc.subjecthuman serum
dc.subjectimmobilized metal affinity chromatography
dc.subjectphosphopeptide enrichment
dc.subjectsyringe type microextration
dc.subjectvinylphosphonic acid
dc.titleTi (IV) attached-phosphonic acid functionalized capillary monolith as a stationary phase for in-syringe-type fast and robust enrichment of phosphopeptides
dc.typeArticle

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