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光敏剂抗体药物偶联物:过去、现在和未来。

Photosensitizer Antibody-Drug Conjugates: Past, Present, and Future.

出版信息

Bioconjug Chem. 2019 Apr 17;30(4):975-993. doi: 10.1021/acs.bioconjchem.9b00055. Epub 2019 Mar 27.

Abstract

This Review aims to highlight key aspects of tetrapyrrole-based antibody-drug conjugates (ADCs) and significant developments in the field since 2010. Many new conjugation methods have been developed and employed in the past decade, and associated with this, there has been a rising interest in theranostic conjugates. We have investigated the physicochemical properties that tetrapyrroles need to possess in order to be viable photosensitizers for conjugation to antibodies. Differences in conjugation strategies are discussed, and structure-activity relationships of tetrapyrrole-antibody conjugates are reported, where available. As the elegance of bioconjugation techniques has increased, it has paved the way for exceptionally phototoxic, yet highly selective, tetrapyrrole-antibody conjugates, with photocytotoxicities in the nanomolar range, to be synthesized and biologically evaluated.

摘要

本综述旨在强调基于四吡咯的抗体药物偶联物(ADC)的关键方面,以及自 2010 年以来该领域的重要进展。过去十年中开发并采用了许多新的偶联方法,并且与此相关的是,治疗诊断偶联物的兴趣日益增加。我们研究了四吡咯需要具备哪些理化性质才能成为可与抗体偶联的可行光敏剂。讨论了偶联策略的差异,并报告了四吡咯-抗体偶联物的结构-活性关系(如有)。随着生物偶联技术的日益完善,为合成和生物学评估具有纳米级光细胞毒性的非常光毒性但高度选择性的四吡咯-抗体偶联物铺平了道路。

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