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采用水溶性氮杂内酯功能化聚合物合成的蛋白质-聚合物缀合物能够实现受体特异性细胞摄取,从而实现靶向药物递送。

Protein-Polymer Conjugates Synthesized Using Water-Soluble Azlactone-Functionalized Polymers Enable Receptor-Specific Cellular Uptake toward Targeted Drug Delivery.

机构信息

Molecular and Cellular Biology Program , University of Massachusetts Amherst , Amherst , Massachusetts 01003 , United States.

出版信息

Bioconjug Chem. 2019 Apr 17;30(4):1220-1231. doi: 10.1021/acs.bioconjchem.9b00155. Epub 2019 Apr 5.

Abstract

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.

摘要

蛋白质与载药聚合物结构的缀合是一种很有吸引力的策略,可以促进各种临床需求的靶向药物递送。目前可用于与蛋白质缀合的聚合物通常对后续药物负载的化学多功能性有限。许多具有用于药物负载的有用化学功能的聚合物通常在水中不溶,这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、氮丙啶基功能化聚合物可以接枝到蛋白质上,与小分子荧光团缀合,然后以受体特异性的方式被细胞内化。使用可逆加成-断裂链转移聚合合成的聚(2-乙烯基-4,4-二甲基氮丙啶),在聚合后用亚化学计量的三乙二醇单甲醚进行修饰,得到反应性的水溶性、氮丙啶基功能化共聚物。然后将这些反应性聚合物与全转铁蛋白和卵转铁蛋白缀合。蛋白质凝胶分析验证了蛋白质成功地与聚合物缀合,并且蛋白质-聚合物缀合物随后使用分子筛层析从未反应的蛋白质和聚合物中纯化出来。使用表面过度表达转铁蛋白受体的乳腺癌细胞系进行的内化实验表明,全转铁蛋白-聚合物缀合物被细胞以与受体介导的内吞作用一致的机制内化。蛋白质-聚合物缀合物的内化表明,蛋白质配体在与聚合物缀合后保持其整体结构和功能。我们的蛋白质-聚合物缀合物合成方法为制备广泛的生物医学应用感兴趣的生物缀合物提供了一种简单、可定制的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5ff/6608588/ae0ae25d2438/nihms-1030307-f0002.jpg

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