Padariya Monikaben, Marek-Trzonkowska Natalia, Kalathiya Umesh
International Centre for Cancer Vaccine Science, University of Gdansk, ul. Kładki 24, 80-822 Gdansk, Poland.
Int J Mol Sci. 2025 Jul 22;26(15):7047. doi: 10.3390/ijms26157047.
Ferritin nanocages with spherical shells carry proteins or antigens that enable their use as highly efficient nanoreactors and nanocarriers. Mimicking the surface Spike (S) receptor-binding domain (RBD) from SARS-CoV-2, ferritin nanocages induce neutralizing antibody production or block viral entry. Herein, by implementing molecular dynamics simulation, we evaluate the efficiency in the interaction pattern (active or alternative sites) of H-ferritin displaying the 24 S RBDs with host-cell-receptor or monoclonal antibodies (mAbs; B38 or VVH-72). Our constructed nanocage targeted the receptor- or antibody-binding interfaces, suggesting that mAbs demonstrate an enhanced binding affinity with the RBD, with key interactions originating from its variable heavy chain. The S RBD interactions with ACE2 and B38 involved the same binding site but led to divergent dynamic responses. In particular, both B38 chains showed that asymmetric fluctuations had a major effect on their engagement with the Spike RBD. Although the receptor increased the binding affinity of VVH-72 for the RBD, the mAb structural orientation on the nanocage remained identical to its conformation when bound to the host receptor. Overall, our findings characterize the essential pharmacophore formed by Spike RBD residues over nanocage molecules, which mediates high-affinity interactions with either binding partner. Importantly, the ferritin-displayed RBD maintained native receptor and antibody binding profiles, positioning it as a promising scaffold for pre-fusion stabilization and protective RBD vaccine design.
具有球形外壳的铁蛋白纳米笼可携带蛋白质或抗原,使其能够用作高效的纳米反应器和纳米载体。模仿严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的表面刺突(S)受体结合域(RBD),铁蛋白纳米笼可诱导中和抗体产生或阻断病毒进入。在此,通过进行分子动力学模拟,我们评估了展示24个S RBD的H-铁蛋白与宿主细胞受体或单克隆抗体(mAb;B38或VVH-72)在相互作用模式(活性或替代位点)方面的效率。我们构建的纳米笼靶向受体或抗体结合界面,这表明单克隆抗体与RBD的结合亲和力增强,关键相互作用源自其可变重链。S RBD与血管紧张素转换酶2(ACE2)和B38的相互作用涉及相同的结合位点,但导致了不同的动态反应。特别是,两条B38链均显示不对称波动对它们与刺突RBD的结合有重大影响。尽管受体增加了VVH-72对RBD的结合亲和力,但纳米笼上的单克隆抗体结构取向与其与宿主受体结合时的构象保持相同。总体而言,我们的研究结果表征了纳米笼分子上由刺突RBD残基形成的基本药效基团,该药效基团介导与任一结合伴侣的高亲和力相互作用。重要的是,铁蛋白展示的RBD保持了天然受体和抗体结合谱,使其成为融合前稳定和保护性RBD疫苗设计的有前途的支架。