Epitope imprinted polyethersulfone beads by self-assembly for target protein capture from the plasma proteome

Polymer self-assembly was developed as an epitope imprinting strategy involving facile processes and high recognition site density. As a model, transferrin epitope imprinted polyethersulfone (PES) beads were successfully fabricated using this technique. The imprinted beads demonstrated excellent sel...

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Bibliographic Details
Published in:Chemical communications (Cambridge, England) England), 2014-08, Vol.50 (67), p.9521-9524
Main Authors: Yang, Kaiguang, Liu, Jianxi, Li, Senwu, Li, Qinran, Wu, Qi, Zhou, Yuan, Zhao, Qun, Deng, Nan, Liang, Zhen, Zhang, Lihua, Zhang, Yukui
Format: Article
Language:English
Subjects:
Adsorption
Animals
Beads
Density
Epitopes - chemistry
Humans
Microspheres
Molecular Imprinting - methods
Polyethersulfones
Polymers - chemical synthesis
Polymers - chemistry
Proteins
Proteome - chemistry
Proteome - immunology
Recognition
Self assembly
Strategy
Sulfones - chemical synthesis
Sulfones - chemistry
Transferrin
Transferrin - chemistry
Transferrin - immunology
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Summary:Polymer self-assembly was developed as an epitope imprinting strategy involving facile processes and high recognition site density. As a model, transferrin epitope imprinted polyethersulfone (PES) beads were successfully fabricated using this technique. The imprinted beads demonstrated excellent selectivity toward the transferrin epitope and transferrin even in the real sample.
ISSN:1359-7345
1364-548X
DOI:10.1039/c4cc03428g