抗体导向酶前药物治疗系统的模块化组装。

IF 3.6 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
ACS Chemical Biology Pub Date : 2026-10-16 Epub Date: 2026-10-01 DOI:10.1021/acschembio.6c00539
Maura E. Charette, Madelyn H. Ratesic, Gianna N. Falcone, Grace V. Lewis, Isabella R. Demyan, Sagar D. Khare, Alexander Deiters
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引用次数: 0

摘要

抗体导向酶前药治疗(ADEPT)利用靶向癌症的抗体-酶偶联物选择性地激活肿瘤部位的前药。我们开发了一种模块化即插即用方法,用于生成ADEPT抗体-酶偶联物,该方法将自标记snaptag -酶融合物与苯基鸟嘌呤标记的抗体配对,以快速生成一系列用于测试的偶联物。这种方法能够融合药物级抗体,这些抗体是使用生物正交自标记化学的重组表达酶进行位点特异性修饰的。ADEPT系统最后组装步骤的双正交性甚至提供了抗体-酶在靶细胞环境中原位配对的能力,提高了测试的便利性,并有可能改善体内药动学。我们已经证明了偶联物的形成和抗原阳性细胞的定位,在偶联细胞表面结合时保留酶活性,并最终选择性杀死肿瘤细胞。此外,这种模块化组装使我们能够通过特定位点的光可切割保护基团的结合来构建条件控制的ADEPT系统,将笼状酶与笼状前药配对以创建布尔与逻辑,通过提供对细胞毒性药物激活的条件控制来潜在地增加治疗窗口。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modular Assembly of Systems for Antibody-Directed Enzyme Prodrug Therapy

Antibody-directed enzyme prodrug therapy (ADEPT) utilizes a cancer-targeting antibody–enzyme conjugate to selectively activate a prodrug at the site of a tumor. We developed a modular plug-and-play approach for the generation of ADEPT antibody–enzyme conjugates that pairs a self-labeling SNAPtag-enzyme fusion with a benzylguanine-tagged antibody for rapid generation of a series of conjugates for testing. This approach enables the fusion of pharmacy-grade antibodies that are site-specifically modified with a recombinantly expressed enzyme using bioorthogonal self-labeling chemistry. The biorthogonality of the final assembly step of the ADEPT system even provides the ability for antibody–enzyme pairing in situ in the target cellular environment, improving ease of testing and potentially improving in vivo pharmokinetics. We have demonstrated conjugate formation and localization to antigen-positive cells, retained enzymatic activity upon conjugate cell surface binding, and ultimately selective killing of tumor cells. Additionally, this modular assembly allowed us to construct conditionally controlled ADEPT systems through site-specific incorporation of a light-cleavable protecting group, pairing a caged enzyme with a caged prodrug to create Boolean AND logic, potentially increasing the therapeutic window by providing conditional control over cytotoxic drug activation.

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来源期刊
ACS Chemical Biology
ACS Chemical Biology 生物-生化与分子生物学
CiteScore
7.50
自引率
5.00%
发文量
353
审稿时长
3.3 months
期刊介绍: ACS Chemical Biology provides an international forum for the rapid communication of research that broadly embraces the interface between chemistry and biology. The journal also serves as a forum to facilitate the communication between biologists and chemists that will translate into new research opportunities and discoveries. Results will be published in which molecular reasoning has been used to probe questions through in vitro investigations, cell biological methods, or organismic studies. We welcome mechanistic studies on proteins, nucleic acids, sugars, lipids, and nonbiological polymers. The journal serves a large scientific community, exploring cellular function from both chemical and biological perspectives. It is understood that submitted work is based upon original results and has not been published previously.
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