Zhu Haoran, Ding Yu
State Key Laboratory of Genetics and Development of Complex Phenotypes, School of Life Sciences, Fudan University, Shanghai 200433, China.
Quzhou Fudan Institute, Quzhou 324002, China.
Biology (Basel). 2025 May 14;14(5):547. doi: 10.3390/biology14050547.
Nanobodies, derived from naturally occurring heavy-chain antibodies in camelids (VHHs) and sharks (Vs), are unique single-domain antibodies that have garnered significant attention in therapeutic, diagnostic, and biotechnological applications due to their small size, stability, and high specificity. This review first traces the historical discovery of nanobodies, highlighting key milestones in their isolation, characterization, and therapeutic development. We then explore their structure-function relationship, emphasizing features like their single-domain architecture and long CDR3 loop that contribute to their binding versatility. Additionally, we examine the growing interest in multiepitope nanobodies, in which binding to different epitopes on the same antigen not only enhances neutralization and specificity but also allows these nanobodies to be used as controllable modules for precise antigen manipulation. This review also discusses the integration of AI in nanobody design and optimization, showcasing how machine learning and deep learning approaches are revolutionizing rational design, humanization, and affinity maturation processes. With continued advancements in structural biology and computational design, nanobodies are poised to play an increasingly vital role in addressing both existing and emerging biomedical challenges.
纳米抗体源自骆驼科动物(VHH)和鲨鱼(Vs)体内天然存在的重链抗体,是独特的单域抗体。由于其尺寸小、稳定性高和特异性强,在治疗、诊断和生物技术应用中备受关注。本综述首先追溯了纳米抗体的历史发现,突出了其分离、表征和治疗开发过程中的关键里程碑。接着,我们探讨了它们的结构-功能关系,强调了诸如单域结构和长互补决定区3(CDR3)环等有助于其结合多样性的特征。此外,我们研究了对多表位纳米抗体日益增长的兴趣,其中与同一抗原上不同表位的结合不仅增强了中和作用和特异性,还使这些纳米抗体能够用作精确操纵抗原的可控模块。本综述还讨论了人工智能在纳米抗体设计和优化中的整合,展示了机器学习和深度学习方法如何彻底改变合理设计、人源化和亲和力成熟过程。随着结构生物学和计算设计的不断进步,纳米抗体有望在应对现有和新出现的生物医学挑战中发挥越来越重要的作用。