化学
单域抗体
生物物理学
纳米颗粒
中和
重组DNA
抗体
纳米技术
蛋白质工程
效力
重链
免疫球蛋白轻链
共焦显微镜
穗蛋白
领域(数学分析)
血浆蛋白结合
毒品携带者
药物输送
链条(单位)
单链可变片段
蛋白质折叠
共焦
组合化学
动力学
噬菌体展示
靶向给药
蛋白质稳定性
免疫球蛋白Fc片段
蛋白质结构
作者
Duc H. T. Le,Jenny van Oostrum,E. Van de Westerlo,Jianhong Wang,Gijs J. Overheul,Ronald P. van Rij,William P. J. Leenders,Jetta J. E. Bijlsma,Ilse Roodink,Jan C. M. van Hest,Wouter P. R. Verdurmen
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2026-01-21
卷期号:27 (2): 1446-1458
标识
DOI:10.1021/acs.biomac.5c02042
摘要
Elastin-like polypeptides (ELPs) are self-assembling recombinant biopolymers that can be precisely engineered to display functional targeting ligands. In this study, we developed ELP-based nanoparticles (NPs) displaying the variable domain of the heavy chain of heavy-chain-only antibodies (VHHs) targeting the SARS-CoV-2 spike protein. By tuning VHH selection, multivalency, and surface display density, we created targeted ELP NPs capable of blocking entry of spike-protein-presenting virus-like particles (VLPs) and live viruses, with subnanomolar IC50 values, significantly outperforming the monovalent VHH equivalents. Notably, optimizing multivalency and VHH density unlocked broad virus-neutralizing potency against multiple variants, including Omicron variants resistant against the monovalent VHH equivalents. Confocal imaging further revealed that VHH-ELP NPs formed aggregates with VLPs, enhancing uptake by M1 macrophages, suggesting potential for eliciting vaccinal effects. Overall, this work highlights the versatility of ELP NPs as a tunable antiviral platform and provides design principles for next-generation nanotherapeutics against evolving viral threats.
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