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dc.contributor.authorChen, Li-Jun
dc.contributor.authorHumphrey, Sean
dc.contributor.authorZhu, Jun-Long
dc.contributor.authorZhu, Fan-Fan
dc.contributor.authorWang, Xu-Qing
dc.contributor.authorWang, Xiang
dc.contributor.authorWen, Jin
dc.contributor.authorYang, Hai-Bo
dc.contributor.authorGale, Philip A.
dc.date.accessioned2022-01-18T03:40:45Z
dc.date.available2022-01-18T03:40:45Z
dc.date.issued2021en_AU
dc.identifier.urihttps://hdl.handle.net/2123/27332
dc.description.abstractThe selective and efficient capture of phosphopeptides is critical for comprehensive and in-depth phosphoproteome analysis. Reported here is a new switchable two-dimensional (2D) supramolecular polymer that can serve as an ideal platform for the enrichment of phos-phopeptides. A well-defined, positively charged metallacycle incorporated into the polymer endows the resultant polymer with a high affinity for phosphopeptides. Importantly, the stimuli-responsive nature of the polymer facilitates switchable binding affinity of phos-phopeptides, thus resulting in excellent performance in phosphopeptide enrichment and separation from model proteins. The polymer has a high enrichment capacity (165 mg/g) and detection sensitivity (2 fmol), high enrichment recovery (88%), excellent specificity, and rapid enrichment and separation properties. Additionally, we have demonstrated the capture of phosphopeptides from the tryptic digest of real bio-samples, thus illustrating the potential of this polymeric material in phosphoproteomic studies.en_AU
dc.language.isoenen_AU
dc.publisherAmerican Chemical Societyen_AU
dc.relation.ispartofJournal of the American Chemical Societyen_AU
dc.rightsCreative Commons Attribution 4.0en_AU
dc.subjectsupramolecular chemistryen_AU
dc.subjectanalytical chemistryen_AU
dc.titleA Two-Dimensional Metallacycle Cross-Linked Switchable Polymer for Fast and Highly Efficient Phosphorylated Peptide Enrichmenten_AU
dc.typeArticleen_AU
dc.subject.asrc0399 Other Chemical Sciencesen_AU
dc.identifier.doi10.1021/jacs.0c12904
dc.type.pubtypeAuthor accepted manuscripten_AU
dc.relation.arcDP180100612
usyd.facultySeS faculties schools::Faculty of Science::School of Chemistryen_AU
usyd.departmentSydneyNanoen_AU
usyd.citation.volume143en_AU
usyd.citation.spage3325en_AU
usyd.citation.epage3339en_AU
workflow.metadata.onlyNoen_AU


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