Talelli Marina, Vicent María J
Polymer Therapeutics Lab, Centro de Investigación Príncipe Felipe (CIPF) , Av. Eduardo Primo Yúfera 3, 46012 Valencia, Spain.
Biomacromolecules. 2014 Nov 10;15(11):4168-77. doi: 10.1021/bm5011883. Epub 2014 Oct 23.
Protein therapeutics have become an important class of medicines for a large variety of diseases. However, they have disadvantages such as rapid elimination/metabolism leading to the need for repeated doses, immunogenicity/antigenicity, and aggregation/degradation during formulation and storage. The concept of polymer masked-unmasked protein therapy (PUMPT) makes use of polymer-protein multivalent conjugation with biodegradable carriers, which mask the protein activity during transport and increase its stability, but is capable of specifically triggering an unmasking effect at the disease site, allowing its therapeutic action. The aim of this study was to widen the PUMPT concept by designing reduction sensitive poly-l-glutamic acid (PGA)-based conjugates, in which the protein release and unmasking effect takes place in the reducing environments found intracellularly as well as in the tumor microenvironment. Lysozyme was used as the model protein to achieve proof of concept. Overall, the synthesized platform showed to be promising for the delivery of anticancer proteins as well as for enzyme replacement therapeutic approaches aiming to treat lysosomal storage disorders.
蛋白质疗法已成为治疗多种疾病的一类重要药物。然而,它们存在一些缺点,如快速消除/代谢导致需要重复给药、免疫原性/抗原性,以及在制剂和储存过程中的聚集/降解。聚合物掩蔽-去掩蔽蛋白疗法(PUMPT)的概念利用了聚合物-蛋白质与可生物降解载体的多价共轭,这种共轭在运输过程中掩蔽蛋白质活性并提高其稳定性,但能够在疾病部位特异性触发去掩蔽效应,从而发挥其治疗作用。本研究的目的是通过设计基于还原敏感型聚-L-谷氨酸(PGA)的共轭物来扩展PUMPT概念,其中蛋白质的释放和去掩蔽效应发生在细胞内以及肿瘤微环境中的还原环境中。使用溶菌酶作为模型蛋白来实现概念验证。总体而言,合成的平台显示出在递送抗癌蛋白以及用于治疗溶酶体贮积症的酶替代治疗方法方面具有前景。