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Preparation of core-shell-type poly(ethylene glycol) grafted polystyrene resins and their characteristics in solid-phase peptide synthesis

机译:核壳型聚乙二醇接枝聚苯乙烯树脂的制备及其在固相肽合成中的特性

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By suspension polymerization using styrene, divinylbenzene, and synthetic poly(ethylene glycol) (PEG) macromers, we have prepared core-shell-type resins that have a highly crosslinked polystyrene core and a PEG shell. The PEG macromonomer, which has a vinyl group and an amino group at each terminal, plays a role as a stabilizer in the suspension polymerization system. All the resins were of the bead type witha diameter of 38-150 mum. The loading capacities of the amino groups were 0.1-0.2 mmol(.)(g(.)resin)(-1) and the thickness of the PEG shell 2-4 mum, which was verified by cross-sectioned views of the fluorescamine-coupled beads. During coupling of amino acids in solid-phase peptide synthesis, the resin showed better yields than TentaGel resin, especially during the first coupling step. In the enzymatic cleavage reaction, the resin-bound peptides were shaved about 5-10 times more than TentaGel resin. [References: 26]
机译:通过使用苯乙烯,二乙烯基苯和合成的聚(乙二醇)(PEG)大分子单体进行悬浮聚合,我们制备了具有高度交联的聚苯乙烯核和PEG壳的核-壳型树脂。在每个末端具有乙烯基和氨基的PEG大分子单体在悬浮聚合体系中起稳定剂的作用。所有树脂均为珠粒类型,直径为38-150微米。氨基的负载量为0.1-0.2 mmol(。)(g(。)树脂)(-1),PEG壳的厚度为2-4毫米,这是通过荧光胺-耦合珠。在固相肽合成中氨基酸偶联过程中,该树脂的收率要高于TentaGel树脂,尤其是在第一步偶联步骤中。在酶促裂解反应中,与TentaGel树脂相比,与树脂结合的肽被剃刮的次数大约是5-10倍。 [参考:26]

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