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Synthesis of Semitelechelic Maleimide Poly(PEGA) for Protein Conjugation By RAFT Polymerization

机译:通过RAFT聚合合成用于蛋白质缀合的半遥远的马来酰亚胺聚(PEGA)

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摘要

Maleimide end functionalized polymers for site-selective conjugation to free cysteines of proteins were synthesized using reversible addition-fragmentation chain transfer (RAFT) polymerization. A furan-protected maleimide chain transfer agent (CTA) was employed in the RAFT polymerization of poly(ethylene glycol) methyl ether acrylate (PEGA). Gel permeation chromatography (GPC) with laser light scattering detection indicated that 20000 and 39000 Da polyPEGA had been made with polydispersity indices of 1.25 and 1.36, respectively. The maleimide group on the polymer chain end was exposed by heating the poly(PEGA)s for 4 h. The deptotection efficiency was estimated to be 80 and 60% for poly(PEGA)2o kDa and poly(PEGA)39 kDa, respectively. Maleimide-poly(PEGA)s were conjugated to V131C T4 lysozyme (T4L), and the resultant polymer-protein conjugates were characterized by size exclusion chromatography and gel electrophoresis.
机译:使用可逆的加成-断裂链转移(RAFT)聚合合成用于位点选择性缀合到蛋白质的半胱氨酸的马来酰亚胺末端官能化聚合物。呋喃保护的马来酰亚胺链转移剂(CTA)用于聚(乙二醇)甲基醚丙烯酸酯(PEGA)的RAFT聚合中。带有激光散射检测的凝胶渗透色谱法(GPC)表明已制备了20000和39000 Da的聚PEGA,其多分散指数分别为1.25和1.36。通过加热聚(PEGA)4小时使聚合物链末端的马来酰亚胺基暴露。估计聚(PEGA)20 kDa和聚(PEGA)39 kDa的检测效率分别为80%和60%。将马来酰亚胺-聚(PEGA)与V131C T4溶菌酶(T4L)偶联,并通过尺寸排阻色谱和凝胶电泳对所得的聚合物-蛋白质偶联物进行表征。

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