首页> 外文OA文献 >Protein immobilization onto poly(acrylic acid) functional\ud macroporous PolyHIPE obtained by surface-initiated ARGET ATRP from multi-tasking amino-polyHIPE precursor.
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Protein immobilization onto poly(acrylic acid) functional\ud macroporous PolyHIPE obtained by surface-initiated ARGET ATRP from multi-tasking amino-polyHIPE precursor.

机译:蛋白质固定在聚丙烯酸功能性\ ud上 从多任务氨基-polyHIPE前体表面引发的ARGET ATRP获得大孔PolyHIPE。

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摘要

Amino-functional macroporous monoliths from polymerized high internal phase emulsion (polyHIPE) were surface modified with initiators for atom transfer radical polymerization (ATRP). The ATRP initiator groups on the polyHIPE surface were successfully used to initiate activator regeneration by electron transfer (ARGET) ATRP of (meth)acrylic monomers, such as methyl methacrylate (MMA) or tert-butyl acrylate (tBA) resulting in a dense coating of polymers on the polyHIPE surface. Addition of sacrificial initiator permitted control of the amount of polymer grafted onto the monolith surface. Subsequent removal of the tert- butyl protecting groups yielded highly functional polyHIPE-g-poly(acrylic acid). The versatility to use the high density of carboxylic acid groups for secondary reactions was demonstrated by the successful conjugation of enhanced green fluorescent protein (eGFP) and coral derived red fluorescent protein (DsRed) using EDC/sulfo-NHS chemistry, on the polymer 3D-scaffold surface. The materials and methodologies presented here are simple and robust, thus, opening new possibilities for the bioconjugation of highly porous polyHIPE for bioseparation applications.
机译:将聚合的高内相乳液(polyHIPE)制备的氨基官能大孔整料用引发剂进行表面改性,以进行原子转移自由基聚合(ATRP)。 polyHIPE表面上的ATRP引发剂基团已成功用于通过电子转移(ARGET)(甲基)丙烯酸单体(如甲基丙烯酸甲酯(MMA)或丙烯酸叔丁酯(tBA))的ATRP引发活化剂再生,从而形成致密的polyHIPE表面的聚合物。牺牲引发剂的加入允许控制接枝到整料表面上的聚合物的量。随后除去叔丁基保护基,得到高官能度的聚HIPE-g-聚(丙烯酸)。通过在聚合物3D-上使用EDC /磺基-NHS化学方法成功结合增强的绿色荧光蛋白(eGFP)和珊瑚衍生的红色荧光蛋白(DsRed),证明了将高密度羧酸基团用于副反应的多功能性。脚手架表面。此处介绍的材料和方法简单,耐用,因此为生物分离应用中的高孔隙度polyHIPE的生物缀合开辟了新的可能性。

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