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首页> 外文期刊>Colloids and Surfaces, B. Biointerfaces >Polymers of 2-methacryloyloxyethyl phosphorylcholine truly work as cell membrane mimic?
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Polymers of 2-methacryloyloxyethyl phosphorylcholine truly work as cell membrane mimic?

机译:2-甲基丙烯酰氧基乙基磷酰胆碱的聚合物真正起到细胞膜模拟的作用吗?

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We have prepared several types of polymers derived from 2-methacryloyloxyethyl phosphorylcholine (MPC) to evaluate whether polymers of MPC work as cell membrane mimic or not. We firstly applied capturing test of target proteins of 4-carboxybenzenesulfonamide (Sul) or ibuprofen (Ibu) as a probe.As the results, the rather hydrophilic polymers based on MPC were able to suppress non-specific binding proteins as expected. Additionally, some of the MPC based polymeric surface was able to capture greater amount of carbonic anhydrase II than those of other polymers, when Sul was utilized as probe. In contrary, all the polymers having PC groups and Ibu probe were unable to capture Cyclooxygenase-1 (COX-1), its target protein. These results suggested that the position of PC groups realized hydrophilic polymer surface, while MPC based polymer was not able to supply the suitable environment for COX-1 to interact with Ibu.
机译:我们准备了几种类型的衍生自2-甲基丙烯酰氧基乙基磷酰胆碱(MPC)的聚合物,以评估MPC的聚合物是否可作为细胞膜模拟物发挥作用。首先,我们以4-羧基苯磺酰胺(Sul)或布洛芬(Ibu)的靶蛋白作为捕获探针进行了捕获测试。结果,基于MPC的相当亲水的聚合物能够按预期抑制非特异性结合蛋白。另外,当使用Sul作为探针时,一些基于MPC的聚合物表面能够捕获比其他聚合物更大的碳酸酐酶II。相反,所有具有PC基团和Ibu探针的聚合物均无法捕获其目标蛋白Cyclooxygenase-1(COX-1)。这些结果表明,PC基团的位置实现了亲水性聚合物表面,而基于MPC的聚合物无法为COX-1与Ibu相互作用提供合适的环境。

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