South China Advanced Institute for Soft Matter Science and Technology, School of Molecular Science and Engineering, South China University of Technology, Guangzhou, 510640, China.
Shanghai Key Laboratory of Regulatory Biology, School of Life Sciences, East China Normal University, Shanghai, 200241, China.
Biomaterials. 2019 Oct;218:119358. doi: 10.1016/j.biomaterials.2019.119358. Epub 2019 Jul 15.
Cytosolic protein delivery offers opportunities to develop protein-based therapeutics specifically modulate intracellular processes, especially those linked to 'undruggable' targets. Since protein molecules are generally membrane-impermeable due to their macromolecular nature and hydrophilic property, carriers are needed to facilitate protein transport through cell membranes. Current delivery techniques usually require chemical modification or genetically engineering on cargo proteins to strengthen the binding affinity between proteins and the carriers. However, these approaches are usually accompanied with complicated syntheses, and the bioactivity of proteins might be irreversibly changed after modification. In this review, we discussed recent advances in the rational design of polymers for cytosolic delivery of native proteins with distinct isoelectric points and sizes. Functional ligands were grafted onto cationic polymers to strengthen the binding affinity between polymers and proteins, and/or to reduce the charge repulsion between cationic polymers during the formation of polymer/protein complexes. The principles of developed polymers in cytosolic protein delivery were intensively discussed. Furthermore, the possibility of developed polymers in the delivery of therapeutic proteins to treat diseases in vivo was evaluated. We hope to provide theoretical and technical supports to the development of polymers for cytosolic protein delivery.
细胞质蛋白递送为开发基于蛋白质的治疗药物提供了机会,这些药物可以专门调节细胞内的过程,特别是那些与“不可成药”靶点相关的过程。由于蛋白质分子由于其大分子性质和亲水性而通常对细胞膜不可渗透,因此需要载体来促进蛋白质穿过细胞膜的运输。目前的递送技术通常需要对货物蛋白进行化学修饰或基因工程改造,以增强蛋白与载体之间的结合亲和力。然而,这些方法通常伴随着复杂的合成,并且在修饰后,蛋白质的生物活性可能会不可逆转地改变。在这篇综述中,我们讨论了最近在合理设计聚合物方面的进展,这些聚合物可用于具有不同等电点和大小的天然蛋白质的细胞质递送。功能性配体被接枝到阳离子聚合物上,以增强聚合物和蛋白质之间的结合亲和力,和/或在形成聚合物/蛋白质复合物时减少阳离子聚合物之间的电荷排斥。还深入讨论了开发的聚合物在细胞质蛋白递送中的原理。此外,还评估了开发的聚合物在体内递送治疗蛋白以治疗疾病的可能性。我们希望为细胞质蛋白递送用聚合物的开发提供理论和技术支持。