Zhang Xiaoying, Diraviyam Thirumalai
College of Veterinary Medicine, Northwest Agriculture and Forestry University, Yangling, 712100, Shaanxi, China.
Department of Microbiology, Karpagam University, Coimbatore, Tamil Nadu, India.
Methods Mol Biol. 2017;1575:3-13. doi: 10.1007/978-1-4939-6857-2_1.
In spite of their widespread applications as therapeutic, diagnostic, and detection agents, the limitations of polyclonal and monoclonal antibodies have enthused scientists to plan for next-generation biomedical agents, the so-called antibody mimetics, which offer many advantages compared to traditional antibodies. Antibody mimetics could be designed through protein-directed evolution or fusion of complementarity-determining regions with intervening framework regions. In the recent decade, extensive progress has been made in exploiting human, butterfly (Pieris brassicae), and bacterial systems to design and select mimetics using display technologies. Notably, some of the mimetics have made their way to market. Numerous limitations lie ahead in developing mimetics for different biomedical usage, particularly for which conventional antibodies are ineffective. This chapter presents a brief overview of the current characteristics, construction, and applications of antibody mimetics.
尽管多克隆抗体和单克隆抗体作为治疗、诊断和检测试剂有着广泛应用,但它们的局限性促使科学家们规划下一代生物医学试剂,即所谓的抗体模拟物,与传统抗体相比,抗体模拟物具有许多优势。抗体模拟物可以通过蛋白质定向进化或互补决定区与中间框架区的融合来设计。在最近十年中,利用人、蝴蝶(粉纹夜蛾)和细菌系统,通过展示技术来设计和筛选模拟物取得了长足进展。值得注意的是,一些模拟物已进入市场。在开发用于不同生物医学用途的模拟物方面,尤其是针对传统抗体无效的用途,仍存在许多限制。本章简要概述了抗体模拟物的当前特性、构建方法及应用。