Laboratory for In Vivo Cellular and Molecular Imaging, ICMI-BEFY/MIMA, Vrije Universiteit Brussel, Brussels, Belgium.
Methods Mol Biol. 2022;2446:395-407. doi: 10.1007/978-1-0716-2075-5_20.
Near-infrared fluorescence molecular imaging has become an established preclinical technique to investigate molecular processes in vivo and to study novel therapies. Furthermore, fluorescence molecular imaging is gaining significant interest from clinicians as an intra-operative guidance tool. This technique makes use of targeted fluorescent tracers as contrast agents that recognize specific biomarkers expressed at the site of disease. Single-domain antibodies have shown to possess excellent properties for in vivo imaging in comparison to conventional antibodies. In this chapter, we describe a method for site-specific conjugation of a near-infrared fluorophore to single-domain antibodies by exploiting cysteine-maleimide chemistry. As opposed to random conjugation, site-specific conjugation results in a homogenously labeled fluorescent tracer and avoids inference with antigen binding.
近红外荧光分子成像已成为一种成熟的临床前技术,可用于研究体内分子过程和研究新的治疗方法。此外,荧光分子成像作为一种术中指导工具正受到临床医生的极大关注。该技术利用靶向荧光示踪剂作为对比剂,识别疾病部位表达的特定生物标志物。与传统抗体相比,单域抗体在体内成像方面表现出优异的性能。在本章中,我们描述了一种通过利用半胱氨酸-马来酰亚胺化学将近红外荧光团特异性连接到单域抗体上的方法。与随机连接相反,特异性连接导致均一标记的荧光示踪剂,并且避免与抗原结合的干扰。