Epitope imprinted polyethersulfone beads by self-assembly for target protein capture from the plasma proteome.
Epitope imprinted polyethersulfone beads by self-assembly for target protein capture from the plasma proteome.
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DOI：
10.1039/c4cc03428g
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发表时间：
2014-07
影响因子：
4.9
通讯作者：
Kaiguang Yang;Jianxi Liu;Senwu Li;Qinran Li;Qi Wu;Yuan Zhou;Qun Zhao;Nan Deng;Zhen Liang;Lihua Zhang;Yukui Zhang
中科院分区：
文献类型：
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作者：
Kaiguang Yang;Jianxi Liu;Senwu Li;Qinran Li;Qi Wu;Yuan Zhou;Qun Zhao;Nan Deng;Zhen Liang;Lihua Zhang;Yukui Zhang
聚合物自组装作为一种表位印迹技术被开发出来，其过程简单，识别位点密度高。作为模型，利用该技术成功制备了转铁蛋白表位印迹聚醚砜（PES）微球。印迹微球对转铁蛋白表位和转铁蛋白具有良好的选择性，即使在实际样品中也是如此。
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.