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Hierarchically templated beads with tailored pore structure for phosphopeptide capture and phosphoproteomics

机译:具有针对磷酸肽捕获和磷酸化蛋白质组学的定制孔结构的分层模板化珠

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摘要

Two templating approaches to produce imprinted phosphotyrosine capture beads with a controllable pore structure are reported and compared with respect to their ability to enrich phosphopeptides from a tryptic peptide mixture. The beads were prepared by the polymerization of urea-based host monomers and crosslinkers inside the pores of macroporous silica beads with both free and immobilized template. In the final step the silica was removed by fluoride etching resulting in mesoporous polymer replicas with narrow pore size distributions, pore diameters approximate to 10 nm and surface area > 260 m(2) g(-1). The beads displayed pronounced phosphotyrosine affinity and selectivity in binding tests using model peptides in acetonitrile rich solutions with a performance surpassing solution polymerized bulk imprinted materials. Tests of the beads for the enrichment of phosphopeptides from tryptic digests of twelve proteins revealed both pY/pS and pY/Y selectivity. This was reflected in a nearly 6-fold increase in the enrichment factor of a 23-mer pY-peptide and pY/pS normalized intensity ratios up to 1.5, when comparing the template mesoporous beads with the bulk materials.
机译:报告了两种模板方法来生产具有可控孔结构的印迹磷酸酪氨酸捕获珠,并就其从胰蛋白酶肽混合物中富集磷酸肽的能力进行了比较。通过在游离和固定模板的大孔二氧化硅珠孔内部聚合脲基主体单体和交联剂来制备珠。在最后一步中,通过氟化物蚀刻去除了二氧化硅,从而得到了介孔聚合物复制品,其孔径分布狭窄,孔径接近10 nm,表面积> 260 m(2)g(-1)。在富含乙腈溶液中使用模型肽进行的结合测试中,珠子显示出明显的磷酸酪氨酸亲和力和选择性,其性能优于溶液聚合的整体印迹材料。珠子从十二种蛋白质的胰蛋白酶消化物中富集的磷酸化肽的测试显示了pY / pS和pY / Y的选择性。当将模板中孔珠粒与散装材料进行比较时,这反映在23-mer pY肽的富集因子增加了近6倍,pY / pS归一化强度比最高达到1.5。

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