Brun Marie-Priscille, Gauzy-Lazo Laurence
Natural Product and Protein Chemistry, Sanofi, Vitry-sur-Seine, France.
Methods Mol Biol. 2013;1045:173-87. doi: 10.1007/978-1-62703-541-5_10.
Currently, the most widely used chemical methodology for the conjugation of drugs to monoclonal antibodies involves either lysine or cysteine residues. In this chapter, several methods for the preparation of antibody-drug conjugates (ADCs) through conjugation of drugs to solvent-exposed ε-amino groups of lysine residues are described. These methods apply to various cytotoxic agents, both tubulin binders and DNA-targeting agents and different types of linkers, cleavable or not, peptidic or disulfide-based, for example.
目前,将药物与单克隆抗体偶联最广泛使用的化学方法涉及赖氨酸或半胱氨酸残基。在本章中,描述了几种通过将药物与赖氨酸残基暴露于溶剂中的ε-氨基偶联来制备抗体-药物偶联物(ADC)的方法。这些方法适用于各种细胞毒性剂,包括微管蛋白结合剂和DNA靶向剂,以及不同类型的连接子,例如可裂解或不可裂解的、基于肽或二硫键的连接子。