网格蛋白
表面改性
内吞作用
部分
药物输送
链霉亲和素
贪婪
生物物理学
纳米技术
靶向给药
材料科学
化学
细胞生物学
生物
生物化学
细胞
立体化学
抗体
物理化学
生物素
免疫学
作者
Hong‐Sik Kim,Jin Ho Bae,Gijeong Kim,Ji‐Joon Song,Hak‐Sung Kim
出处
期刊:Small
[Wiley]
日期:2022-12-01
卷期号:19 (8)
标识
DOI:10.1002/smll.202204620
摘要
Abstract Protein assemblies have drawn much attention as platforms for biomedical applications, including gene/drug delivery and vaccine, due to biocompatibility and functional diversity. Here, the construction and functionalization of a protein assembly composed of human clathrin heavy chain and light chain for a targeted protein delivery, is presented. The clathrin heavy and light chains are redesigned and associated with each other, and the resulting triskelion unit further self‐assembled into a clathrin assembly with the size of about 28 nm in diameter. The clathrin assembly is dual‐functionalized with a protein cargo and a targeting moiety using two different orthogonal protein–ligand pairs through one‐pot reaction. The functionalized clathrin assembly exhibits about a 900‐fold decreased K D value for a cell‐surface target due to avidity compared to a native targeting moiety. The utility of the clathrin assembly is demonstrated by an efficient delivery of a protein cargo into tumor cells in a target‐specific manner, resulting in a strong cytotoxic effect. The present approach can be used in the creation of protein assemblies with multimodality.
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