Department of Chemical Sciences, University of Naples "Federico II", University of Napoli Federico II Complesso Universitario Monte Sant'Angelo, Via Cintia, 80126 Naples, Italy.
Institute of Applied Sciences and Intelligent Systems (ISASI), Naples Cryo Electron Microscopy Laboratory - EYE LAB, National Research Council (CNR), Via Pietro Castellino 111, 80131 Naples, Italy.
Int J Biol Macromol. 2024 Oct;277(Pt 2):134373. doi: 10.1016/j.ijbiomac.2024.134373. Epub 2024 Jul 31.
Ferritins are natural proteins which spontaneously self-assemble forming hollow nanocages physiologically deputed to iron storage and homeostasis. Thanks to their high stability and easy production in vitro, ferritins represent an intriguing system for nanobiotechnology. Here we investigated the mechanism of disassembly and reassembly of a human recombinant ferritin constituted by the heavy chain (hHFt) exploiting a new procedure which involves the use of minimal amounts of sodium dodecyl sulfate (SDS) and assessed its effectiveness in comparison with two commonly used protocols based on pH shift at highly acidic and alkaline values. The interest in this ferritin as drug nanocarrier is related to the strong affinity of the human H-chain for the transferrin receptor TfR-1, overexpressed in several tumoral cell lines. Using different techniques, like NMR, TEM and DLS, we demonstrated that the small concentrations of SDS can eliminate the nanocage architecture without detaching the monomers from each other, which instead remain strongly associated. Following this procedure, we encapsulated into the nanocage a small ruthenium complex with a remarkable improvement with respect to previous protocols in terms of yield, structural integrity of the recovered protein and encapsulation efficiency. In our opinion, the extensive network of interchain interactions preserved during the SDS-based disassembly procedure represents the key for a complete and correct hHFt reassembly.
铁蛋白是天然蛋白质,它们会自动自组装形成空心纳米笼,在生理上负责储存和维持铁的平衡。由于其高度稳定和易于在体外生产,铁蛋白成为纳米生物技术的一个有趣系统。在这里,我们利用一种新的程序研究了由重链 (hHFt) 组成的人重组铁蛋白的拆解和组装机制,该程序涉及使用少量的十二烷基硫酸钠 (SDS),并评估了其与两种常用的基于高酸性和碱性值 pH 转移的方案相比的有效性。这种铁蛋白作为药物纳米载体的兴趣与人类 H 链对转铁蛋白受体 TfR-1 的强烈亲和力有关,TfR-1 在多种肿瘤细胞系中过度表达。使用不同的技术,如 NMR、TEM 和 DLS,我们证明了少量 SDS 可以消除纳米笼结构,而不会将单体彼此分离,这些单体仍然强烈结合。按照这个程序,我们将一种小的钌配合物封装到纳米笼中,与以前的方案相比,在产率、回收蛋白的结构完整性和封装效率方面都有显著提高。在我们看来,在基于 SDS 的拆解过程中保持的广泛的链间相互作用网络是实现 hHFt 完全正确组装的关键。