多价人工抗体和抗体-药物偶联物的即插即用定制自组装蛋白质平台

Yuzhe Chen, Yunchuan Huang, Shisheng Wang, Xinyuan Wang, Hongyu Lu, Jie Chen, Jing Li, Zhuo Chen, Zhao Li, Tianshan She, Youmei Jin, Yuanping Gao, Jie Zhang, Lijun Wang, Wenjuan Zeng, Hong Zhu, Ze Tao, Prof. Xiaofeng Lu, Prof. Hao Yang
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引用次数: 0

摘要

精确调节药代动力学和药理学性质的多价治疗药物的模块化组装仍然是药物开发中的一个关键挑战。在这里,我们提出了ATPlug,一个自组装蛋白质平台,集成了三个关键的功能模块:三聚化结构域,提高亲和度;SpyCatcher模块,有效的结合;白蛋白结合结构域,优化药代动力学和组织选择性。这种合理的设计促进了多价人工抗体和抗体-药物偶联物(adc)的模块化组装,通过成功结合多种针对表皮生长因子受体(EGFR)、程序性细胞死亡配体1 (PD-L1)和血管内皮生长因子(VEGF)的治疗模块,展示了显著的多功能性。通过内源性白蛋白搭便车,三价结构体的靶结合度提高了30倍,并延长了血浆半衰期。值得注意的是,atplug定制的模块化adc对EGFR的结合亲和力为1.8 nM,并对过表达EGFR的肿瘤细胞表现出选择性细胞毒性,具有强大的肿瘤抑制作用。这种即插即用策略为结合定制多价和多药协同作用的下一代治疗提供了框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Self-Assembled Protein Platform for Plug-and-Play Customization of Multivalent Artificial Antibodies and Antibody-Drug Conjugates

A Self-Assembled Protein Platform for Plug-and-Play Customization of Multivalent Artificial Antibodies and Antibody-Drug Conjugates

Modular assembly of multivalent therapeutics with precise modulation of pharmacokinetic and pharmacological properties remains a critical challenge in drug development. Here, we present ATPlug, a self-assembling protein platform that integrates three crucial functional modules: a trimerization domain to enhance avidity, a SpyCatcher module for efficient conjugation, and an albumin-binding domain to optimize pharmacokinetics and tissue selectivity. This rational design facilitates the modular assembly of multivalent artificial antibodies and antibody-drug conjugates (ADCs), demonstrating remarkable versatility through the successful incorporation of diverse therapeutic modules targeting epidermal growth factor receptor (EGFR), programmed cell death ligand 1 (PD-L1), and vascular endothelial growth factor (VEGF). The trivalent constructs exhibited up to 30-fold enhancement in target binding avidity and extended plasma half-life via endogenous albumin hitchhiking. Notably, the ATPlug-customized modular ADCs achieved binding affinities of 1.8 nM for EGFR and exhibited selective cytotoxicity toward EGFR-overexpressing tumor cells, resulting in potent tumor suppression efficacy. This plug-and-play strategy provides a framework for next-generation therapeutics combining customized multivalency with multidrug synergies.

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来源期刊
Angewandte Chemie
Angewandte Chemie 化学科学, 有机化学, 有机合成
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