Zappala Fabiana, Tsourkas Andrew
Department of Bioengineering, University of Pennsylvania, Philadelphia, PA, USA.
Methods Mol Biol. 2019;2033:275-286. doi: 10.1007/978-1-4939-9654-4_18.
The high specificity and strong binding affinity of antibodies, most commonly immunoglobulin G (IgG), have led to their use in a wide range of research, diagnostic and therapeutic applications. Many of these applications require the antibody to be labeled with additional chemical or biological moieties. Here, we describe a method for the rapid and site-specific labeling of nearly any "off-the-shelf" IgG. Our method utilizes small photoreactive antibody-binding domains (pAbBDs) that are produced by modifying the IgG-binding domains of Protein A and Protein G with the unnatural amino acid benzoylphenylalanine (BPA). The pAbBDs are covalently linked to IgG heavy chains upon exposure to ultraviolet light. Fusion of pAbBDs to a given protein of interest or conjugation of pAbBDs with drugs, fluorophores, and/or other chemical moieties, enables the facile production of a diverse range of antibody conjugates.
抗体(最常见的是免疫球蛋白G,即IgG)具有高特异性和强结合亲和力,这使其在广泛的研究、诊断和治疗应用中得到了使用。这些应用中的许多都要求抗体用额外的化学或生物部分进行标记。在这里,我们描述了一种对几乎任何“现成的”IgG进行快速且位点特异性标记的方法。我们的方法利用了小的光反应性抗体结合结构域(pAbBDs),这些结构域是通过用非天然氨基酸苯甲酰苯丙氨酸(BPA)修饰蛋白A和蛋白G的IgG结合结构域而产生的。在暴露于紫外光时,pAbBDs与IgG重链共价连接。将pAbBDs与特定的目标蛋白融合,或将pAbBDs与药物、荧光团和/或其他化学部分偶联,能够轻松生产出各种各样的抗体偶联物。