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首页> 外文期刊>Biomacromolecules >Synthesis of Surface-Anchored DNA-Polymer Bioconjugates Using Reversible Addition-Fragmentation Chain Transfer Polymerization
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Synthesis of Surface-Anchored DNA-Polymer Bioconjugates Using Reversible Addition-Fragmentation Chain Transfer Polymerization

机译:可逆加成-断裂链转移聚合法合成表面锚定的DNA-聚合物生物共轭物

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We report here an approach to grafting DNA-polymer bioconjugates on a planar solid support using reversible addition-fragmentation chain transfer (RAFT) polymerization. In particular, a trithiocarbonate compound as the RAFT chain transfer agent (CTA) is attached to the distal point of a surface-immobilized oligonucleotide. Initiation of RAFT polymerization, leads to controlled growth of polymers atop DNA molecules on the surface. Growth kinetics of poly(monomethoxy-capped oligofethylene glycol) methacrylate) atop DNA molecules is investigated by monitoring the change of polymer film thickness as a function of reaction time. The reaction conditions, including the polymerization temperature, the initiator concentration, the CTA surface density, and the selection of monomers, are varied to examine their impacts on the grafting efficiency of DNA-polymer conjugates. Comparing to polymer growth atop small molecules, the experimental results suggest that DNA molecules significantly accelerate polymer growth, which is speculated as a result of the presence of highly charged DNA backbones and purine/pyrimidine moieties surrounding the reaction sites.
机译:我们在这里报告了一种使用可逆加成-断裂链转移(RAFT)聚合将DNA-聚合物生物共轭物接枝到平面固体支持物上的方法。尤其是,将三硫代碳酸酯化合物作为RAFT链转移剂(CTA)连接到表面固定的寡核苷酸的末端。 RAFT聚合的引发导致表面上DNA分子顶部的聚合物受控生长。通过监测聚合物膜厚度随反应时间的变化,研究了聚(单甲氧基封端的低聚乙二醇甲基丙烯酸甲酯)在DNA分子上的生长动力学。改变反应条件,包括聚合温度,引发剂浓度,CTA表面密度和单体选择,以检查它们对DNA-聚合物共轭物接枝效率的影响。与小分子顶部的聚合物生长相比,实验结果表明DNA分子显着促进了聚合物的生长,这推测是由于反应位点周围存在带高电荷的DNA主链和嘌呤/嘧啶部分所致。

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