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首页> 外文期刊>Bioconjugate Chemistry >Protein-Polymer Conjugates Synthesized Using Water-Soluble Azlactone-Functionalized Polymers Enable Receptor-Specific Cellular Uptake toward Targeted Drug Delivery
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Protein-Polymer Conjugates Synthesized Using Water-Soluble Azlactone-Functionalized Polymers Enable Receptor-Specific Cellular Uptake toward Targeted Drug Delivery

机译:使用水溶性氮杂物官能化聚合物合成的蛋白质 - 聚合物缀合物使受体特异性细胞摄取能够朝向靶向药物递送

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Conjugation of proteins to drug-loaded polymeric structures is an attractive strategy for facilitating target-specific drug delivery for a variety of clinical needs. Polymers currently available for conjugation to proteins generally have limited chemical versatility for subsequent drug loading. Many polymers that do have chemical functionality useful for drug loading are often insoluble in water, making it difficult to synthesize functional protein-polymer conjugates for targeted drug delivery. In this work, we demonstrate that reactive, azlactone-functionalized polymers can be grafted to proteins, conjugated to a small-molecule fluorophore, and subsequently internalized into cells in a receptor-specific manner. Poly(2-vinyl-4,4-dimethylazlactone), synthesized using reversible addition-fragmentation chain transfer polymerization, was modified post-polymerization with substoichiometric equivalents of triethylene glycol monomethyl ether to yield reactive water-soluble, azlactone-functionalized copolymers. These reactive polymers were then conjugated to proteins holo-transferrin and ovotransferrin. Protein gel analysis verified successful conjugation of proteins to polymer, and protein-polymer conjugates were subsequently purified from unreacted proteins and polymers using size exclusion chromatography. Internalization experiments using a breast cancer cell line that overexpresses the transferrin receptor on its surface showed that the holo-transferrin-polymer conjugate was successfully internalized by cells in a mechanism consistent with receptor-mediated endocytosis. Internalization of protein-polymer conjugate demonstrated that the protein ligand maintained its overall structure and function following conjugation to polymer. Our approach to protein-polymer conjugate synthesis offers a simple, tailorable strategy for preparing bioconjugates of interest for a broad range of biomedical applications.
机译:蛋白质与药物负载的聚合物结构的缀合是一种有吸引力的策略,可促进针对各种临床需求的靶特异性药物递送。目前可用于蛋白质的聚合物通常对随后的药物负载具有有限的化学多功能性。许多确实具有用于药物载荷的化学功能的聚合物通常不溶于水,使得难以合成用于靶向药物递送的功能性蛋白质聚合物缀合物。在这项工作中,我们证明了反应性,偶氮酮官能化聚合物可以接枝到蛋白质,与小分子荧光团缀合,随后以受体特异性方式内化到细胞中。合成的使用可逆添加 - 碎片链转移聚合合成的聚(2-乙烯基-4,4-二甲基唑烷酮)与三乙二醇单甲醚的倒亚乙二醇单甲基醚的倒入聚合后修饰,得到反应性水溶性的唑酯官能化共聚物。然后将这些反应性聚合物与蛋白质Holo-Transferrin和Ovotransferrin缀合。蛋白质凝胶分析验证了蛋白质与聚合物的成功缀合,随后使用尺寸排阻色谱法从未反应的蛋白质和聚合物纯化蛋白质 - 聚合物缀合物。使用过表达转铁蛋白受体的乳腺癌细胞系在其表面上的内化实验表明,通过细胞在与受体介导的内吞作用一致的机制中成功地内化了Holo-Transionrin-聚合物缀合物。蛋白质 - 聚合物缀合物的内化证明蛋白质配体保持其整体结构和功能后缀合与聚合物。我们对蛋白质 - 聚合物共轭物合成的方法提供了一种简单,可定制的策略,用于为广泛的生物医学应用程序制备感兴趣的生物缀合物。

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