Synthesis and characterization of biotin chain-end functionalized boronic acid-containing polymer (boropolymer) as functional glyco-affinity macroligand

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Abstract

A biotin chain-end functionalized boronic acid-containing polymer (biotin boropolymer) as an oriented glyco-affinity macroligand for efficient carbohydrate and glycoconjugate purification and identification application was described. Briefly, the biotin boropolymer was synthesized via a biotin derivated arylamine initiated cyanoxyl-mediated free-radical polymerization in one-pot fashion. The specific streptavidin binding capacity of biotin boropolymer was confirmed by streptavidin-HABA assay, while the specific carbohydrate binding capacity of biotin boropolymer was evaluated by Alizarin Red S binding assay. Efficient glyco-capturing followed by direct MALDI mass spectrometry identification of the captured carbohydrate was demonstrated by using magnetic bead functionalized with the biotin boropolymer via streptavidin/biotin interaction. © 2010 Elsevier Ltd. All rights reserved.
Original languageEnglish
Pages (from-to)471-476
Number of pages6
JournalReactive and Functional Polymers
Volume70
Issue number7
DOIs
StatePublished - Jul 1 2010

Keywords

  • Biotin
  • Boronic acid
  • Carbohydrate
  • Cyanoxyl-mediated free-radical polymerization
  • Glyco-affinity
  • MALDI-mass spectrometry

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