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末端磷酸化三嵌段聚醚作为模板和孔形成剂用于靶向磷酸肽的整体材料表面分子印迹。

Terminally Phosphorylated Triblock Polyethers Acting Both as Templates and Pore-Forming Agents for Surface Molecular Imprinting of Monoliths Targeting Phosphopeptides.

作者信息

Huynh Chau Minh, Arribas Díez Ignacio, Thi Hien Kim Le, Jensen Ole N, Sellergren Börje, Irgum Knut

机构信息

Department of Chemistry, Umeå University, S-901 87 Umeå, Sweden.

Department of Biochemistry & Molecular Biology and VILLUM Center for Bioanalytical Sciences, University of Southern Denmark, Campusvej 55, DK-5230 Odense M, Denmark.

出版信息

ACS Omega. 2023 Feb 20;8(9):8791-8803. doi: 10.1021/acsomega.3c00007. eCollection 2023 Mar 7.

Abstract

The novel process reported here described the manufacture of monolithic molecularly imprinted polymers (MIPs) using a terminally functionalized block copolymer as the imprinting template and pore-forming agent. The MIPs were prepared through a step-growth polymerization process using a melamine-formaldehyde precondensate in a biphasic solvent system. Despite having a relatively low imprinting factor, the use of MIP monolith in liquid chromatography demonstrated the ability to selectively target desired analytes. An MIP capillary column was able to separate monophosphorylated peptides from a tryptic digest of bovine serum albumin. Multivariate data analysis and modeling of the phosphorylated and nonphosphorylated peptide retention times revealed that the number of phosphorylations was the strongest retention contributor for peptide retention on the monolithic MIP capillary column.

摘要

本文报道的新方法描述了使用末端功能化嵌段共聚物作为印迹模板和成孔剂来制造整体式分子印迹聚合物(MIP)。MIP通过在双相溶剂体系中使用三聚氰胺 - 甲醛预缩合物的逐步增长聚合过程制备。尽管印迹因子相对较低,但在液相色谱中使用MIP整体柱证明了能够选择性地靶向所需分析物。MIP毛细管柱能够从牛血清白蛋白的胰蛋白酶消化物中分离出单磷酸化肽段。对磷酸化和非磷酸化肽段保留时间的多变量数据分析和建模表明,磷酸化的数量是肽段在整体式MIP毛细管柱上保留的最强保留贡献因素。

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