LifeArc, Accelerator Building, Open Innovation Campus, Stevenage, SG1 2FX, UK.
Chembiochem. 2019 Mar 15;20(6):754-758. doi: 10.1002/cbic.201800623. Epub 2019 Feb 7.
Antibody-drug conjugates (ADCs) are a growing class of therapeutics that harness the specificity of antibodies and the cell-killing potency of small-molecule drugs. Beyond cytotoxics, there are few examples of the application of an ADC approach to difficult drug discovery targets. Here, we present the initial development of a non-internalising ADC, with a view to selectively inhibiting an extracellular protein. Employing the wellinvestigated matrix metalloproteinase-9 (MMP-9) as our model, we adapted a broad-spectrum, nonselective MMP inhibitor for conjugation and linked this to a MMP-9-targeting antibody. The resulting ADC fully inhibits MMP-9, and ELISA results suggest antibody targeting can direct a nonselective inhibitor.
抗体药物偶联物(ADCs)是一类日益增长的治疗药物,利用了抗体的特异性和小分子药物的细胞杀伤效力。除细胞毒素外,很少有应用 ADC 方法来解决困难的药物发现靶点的例子。在这里,我们介绍了一种非内化 ADC 的初步开发,旨在选择性抑制细胞外蛋白。我们选择了经过充分研究的基质金属蛋白酶-9(MMP-9)作为模型,将一种广谱、非选择性的 MMP 抑制剂进行了修饰,使其与 MMP-9 靶向抗体结合。得到的 ADC 完全抑制了 MMP-9,ELISA 结果表明抗体靶向可以引导非选择性抑制剂。