Grünewald Jan, Brock Ansgar, Geierstanger Bernhard H
Biotherapeutics, Genomics Institute of the Novartis Research Foundation, San Diego, CA, USA.
Methods Mol Biol. 2019;2012:237-278. doi: 10.1007/978-1-4939-9546-2_13.
4'-Phosphopantetheinyl transferases (PPTases) have been employed by researchers as versatile biocatalysts for the site-specific modification of numerous protein targets with structurally diverse molecules. Here we describe the use of these enzymes for the production of homogeneous antibody-drug conjugates (ADCs), which have garnered much attention as innovative anticancer drugs. The exceptionally broad substrate tolerance of PPTases allows for one-step and two-step conjugation strategies for site-specific ADC synthesis. While one-step conjugation involves direct coupling of a drug molecule to an antibody, two-step conjugation provides increased flexibility and efficiency of the conjugation process by first attaching a bioorthogonal chemical handle that is then used for drug molecule attachment in a second step. The aim of this chapter is to outline detailed protocols for both labeling procedures, as well as to provide guidance on enzyme and substrate preparation.
4'-磷酸泛酰巯基乙胺基转移酶(PPTases)已被研究人员用作多功能生物催化剂,用于用结构多样的分子对众多蛋白质靶点进行位点特异性修饰。在此,我们描述了使用这些酶来生产均一的抗体-药物偶联物(ADC),作为创新的抗癌药物,ADC已备受关注。PPTases具有异常广泛的底物耐受性,这使得位点特异性ADC合成可以采用一步法和两步法偶联策略。一步法偶联是指将药物分子直接与抗体偶联,而两步法偶联则是通过首先连接一个生物正交化学手柄,然后在第二步中用于连接药物分子,从而提高了偶联过程的灵活性和效率。本章的目的是概述这两种标记程序的详细方案,并提供有关酶和底物制备的指导。