Samanta Debasis, McRae Samantha, Cooper Beth, Hu Yunxia, Emrick Todd, Pratt Jeanne, Charles Stephen A
Polymer Science and Engineering Department, University of Massachusetts, 120 Governors Drive, Amherst, Massachusetts 01003, USA.
Biomacromolecules. 2008 Oct;9(10):2891-7. doi: 10.1021/bm8006715. Epub 2008 Sep 25.
Polymer-protein conjugation was performed using N-hydroxysuccinimide and aldehyde-terminated zwitterionic polymers, and the resulting polymer-protein conjugates were characterized by gel electrophoresis and fast protein liquid chromatography. Methacryloyloxyethyl phosphorylcholine (MPC) polymers were prepared by atom transfer radical polymerization in which the requisite functional end-groups for protein conjugation were embedded within the polymerization initiators. These phosphorylcholine polymers were conjugated to lysozyme as a model protein, as well as two therapeutic proteins, granulocyte colony stimulating factor (G-CSF) and erythropoietin (EPO). These MPC polymer-protein conjugates represent alternatives to PEGylated proteins, with the potential to provide improved efficacy in a therapeutic treatment relative to the protein itself.
使用N-羟基琥珀酰亚胺和醛基封端的两性离子聚合物进行聚合物-蛋白质偶联,所得的聚合物-蛋白质偶联物通过凝胶电泳和快速蛋白质液相色谱进行表征。甲基丙烯酰氧乙基磷酰胆碱(MPC)聚合物通过原子转移自由基聚合制备,其中用于蛋白质偶联的必需官能端基嵌入在聚合引发剂中。这些磷酰胆碱聚合物与作为模型蛋白的溶菌酶以及两种治疗性蛋白,即粒细胞集落刺激因子(G-CSF)和促红细胞生成素(EPO)进行偶联。这些MPC聚合物-蛋白质偶联物代表了聚乙二醇化蛋白质的替代物,相对于蛋白质本身,有可能在治疗中提供更高的疗效。