LabGenius, London, UK.
MAbs. 2024 Jan-Dec;16(1):2341443. doi: 10.1080/19420862.2024.2341443. Epub 2024 Apr 26.
The development of bispecific antibodies that bind at least two different targets relies on bringing together multiple binding domains with different binding properties and biophysical characteristics to produce a drug-like therapeutic. These building blocks play an important role in the overall quality of the molecule and can influence many important aspects from potency and specificity to stability and half-life. Single-domain antibodies, particularly camelid-derived variable heavy domain of heavy chain (VHH) antibodies, are becoming an increasingly popular choice for bispecific construction due to their single-domain modularity, favorable biophysical properties, and potential to work in multiple antibody formats. Here, we review the use of VHH domains as building blocks in the construction of multispecific antibodies and the challenges in creating optimized molecules. In addition to exploring traditional approaches to VHH development, we review the integration of machine learning techniques at various stages of the process. Specifically, the utilization of machine learning for structural prediction, lead identification, lead optimization, and humanization of VHH antibodies.
双特异性抗体的开发需要将至少两种不同的结合域结合在一起,这些结合域具有不同的结合特性和物理特性,从而产生一种类似药物的治疗药物。这些构建块在分子的整体质量中起着重要作用,并可以影响许多重要方面,从效力和特异性到稳定性和半衰期。由于单域抗体,特别是骆驼科来源的重链可变重链域(VHH)抗体的单域模块化、有利的物理特性以及在多种抗体形式中发挥作用的潜力,它们成为双特异性构建的越来越受欢迎的选择。在这里,我们回顾了 VHH 结构域作为多特异性抗体构建的构建块的用途,以及在创建优化分子方面所面临的挑战。除了探索 VHH 开发的传统方法外,我们还回顾了机器学习技术在该过程各个阶段的整合。具体来说,利用机器学习进行结构预测、先导化合物识别、先导化合物优化以及 VHH 抗体的人源化。