单域抗体
模块化(生物学)
计算机科学
领域(数学分析)
计算生物学
双特异性抗体
鉴定(生物学)
抗体
过程(计算)
生物
单克隆抗体
数学
免疫学
遗传学
数学分析
植物
操作系统
作者
Michael Mullin,James McClory,Winston Haynes,Justin Grace,N.J. Robertson,Gino Van Heeke
出处
期刊:mAbs
[Informa]
日期:2024-04-26
卷期号:16 (1): 2341443-2341443
被引量:15
标识
DOI:10.1080/19420862.2024.2341443
摘要
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.
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