Osiński Norbert, Majsterkiewicz Karolina, Pakosz-Stępień Zuzanna, Azuma Yusuke, Biela Artur P, Gaweł Szymon, Heddle Jonathan G
Malopolska Centre of Biotechnology, Jagiellonian University, Gronostajowa 7A, Kraków, 30387, Poland.
Doctoral School of Exact and Natural Sciences, Jagiellonian University, Łojasiewicza 11, Kraków, 30384, Poland.
Macromol Rapid Commun. 2025 Apr;46(6):e2400712. doi: 10.1002/marc.202400712. Epub 2024 Dec 16.
The rational design and production of a novel series of engineered protein cages are presented, which have emerged as versatile and adaptable platforms with significant applications in biomedicine. These protein cages are assembled from multiple protein subunits, and precise control over their interactions is crucial for regulating assembly and disassembly, such as the on-demand release of encapsulated therapeutic agents. This approach employs a homo-undecameric, ring-shaped protein scaffold with strategically positioned metal binding sites. These engineered proteins can self-assemble into highly stable cages in the presence of cobalt or zinc ions. Furthermore, the cages can be disassembled on demand by employing external triggers such as chelating agents and changes in pH. Interestingly, for certain triggers, the disassembly process is reversible, allowing the cages to reassemble upon reversal or outcompeting of triggering conditions/agents. This work offers a promising platform for the development of advanced drug delivery systems and other biomedical applications.
本文介绍了一系列新型工程蛋白笼的合理设计与生产,这些蛋白笼已成为具有重要生物医药应用的多功能且适应性强的平台。这些蛋白笼由多个蛋白质亚基组装而成,精确控制它们之间的相互作用对于调节组装和解组装至关重要,例如按需释放封装的治疗剂。这种方法采用了一种具有战略定位金属结合位点的同型十一聚体环状蛋白支架。这些工程蛋白在钴或锌离子存在下可自组装成高度稳定的笼子。此外,通过使用螯合剂和pH值变化等外部触发因素,笼子可按需拆解。有趣的是,对于某些触发因素,拆解过程是可逆的,使笼子在触发条件/试剂逆转或被竞争掉后能够重新组装。这项工作为先进药物递送系统及其他生物医药应用的开发提供了一个有前景的平台。