结合
化学
生物正交化学
共轭体系
小分子
组织蛋白酶B
分子
蛋白酶
组合化学
劈理(地质)
生物化学
组织蛋白酶
酶
细胞内
肽
癌细胞
生物物理学
立体化学
转染
组织蛋白酶
伏立诺他
生物相容性材料
寡肽
组织蛋白酶D
单克隆抗体
拟肽
免疫毒素
纳米技术
分子探针
药物输送
适体
作者
Inga Černauskienė,E. Izquierdo,Sarah Keller,Harley D. Betts,Kevin Cariou,Vicente Marchán,Gilles Gasser,Gonçalo J. L. Bernardes
标识
DOI:10.1002/anie.202513808
摘要
Carbon monoxide (CO) has shown therapeutic potential across various diseases, including cancer. To enable controlled delivery, many CO-releasing molecules (CORMs) have been developed. However, their clinical translation has been limited due to concerns about stability, potential toxicity, and insufficient targeting ability. In this study, we report the synthesis and characterization of an enzyme-triggered CO-releasing molecule (ET-CORM) that can be site-specifically conjugated to antibodies. This novel ET-CORM is built on a biocompatible iron core, and releases CO upon cleavage by the cancer-associated protease cathepsin B (CatB). The incorporation of a bioorthogonal handle into ET-CORM enabled its efficient and site-specific conjugation to the clinically used antibody trastuzumab via the interchain disulfide bonds. The resulting ET-CORM-antibody conjugate (ET-CORM-Ab) exhibited an average drug-to-antibody ratio (DAR) of 6.8, corresponding to approximately 20 CO molecules per conjugate. This construct allowed for selective intracellular CO delivery to HER2-overexpressing and CatB-expressing cells in vitro. This study represents a metal-based CORM-antibody conjugate activated by a tumor-associated enzymatic trigger, opening new avenues for investigating CO-mediated effects and advancing CO-based cancer therapies to the clinics.
科研通智能强力驱动
Strongly Powered by AbleSci AI