Spoendlin Fabian C, Deane Charlotte M
Oxford Protein Informatics Group, Department of Statistics, University of Oxford, Oxford, UK.
Methods Mol Biol. 2025;2937:261-274. doi: 10.1007/978-1-0716-4591-8_16.
Computational epitope profiling methods group antibodies that bind to the same epitope. They can be used to predict epitopes and reduce the number of antibodies that need to be characterized experimentally. Conventionally, computational epitope profiling is achieved by clustering antibodies by sequence similarity. While sequence-similar antibodies are likely to share a common function, such methods neglect that antibodies with highly diverse sequences can exhibit similar binding site geometries and engage common epitopes. The SPACE2 algorithm described here is an epitope profiling method that clusters antibodies based on the structural similarity of models predicted with a state-of-the-art protein structure prediction tool. SPACE2 accurately clusters antibodies that engage the same epitope and exhibits far greater data coverage than conventional methods. Furthermore, SPACE2 detects signals of functional convergence and, unlike sequence-based methods, is able to link antibodies diverse in sequence, genetic lineage, and species origin. These results reiterate that structural data provides orthogonal information to sequence and improves our ability to study antibodies and their epitopes.
计算表位分析方法将结合相同表位的抗体分组。它们可用于预测表位,并减少需要通过实验进行表征的抗体数量。传统上,计算表位分析是通过按序列相似性对抗体进行聚类来实现的。虽然序列相似的抗体可能具有共同的功能,但这种方法忽略了序列高度不同的抗体可能表现出相似的结合位点几何形状并结合共同的表位。这里描述的SPACE2算法是一种表位分析方法,它基于使用最先进的蛋白质结构预测工具预测的模型的结构相似性对抗体进行聚类。SPACE2能准确地将结合相同表位的抗体聚类,并且与传统方法相比,具有更大的数据覆盖范围。此外,SPACE2能检测到功能趋同的信号,并且与基于序列的方法不同,它能够将序列、遗传谱系和物种来源不同的抗体联系起来。这些结果重申,结构数据为序列提供了正交信息,并提高了我们研究抗体及其表位的能力。