Michalewicz Kevin, Barahona Mauricio, Bravi Barbara
Department of Mathematics, Imperial College London, London SW7 2AZ, UK.
Department of Mathematics, Imperial College London, London SW7 2AZ, UK.
Structure. 2024 Dec 5;32(12):2422-2434.e5. doi: 10.1016/j.str.2024.10.001. Epub 2024 Oct 25.
The high binding affinity of antibodies toward their cognate targets is key to eliciting effective immune responses, as well as to the use of antibodies as research and therapeutic tools. Here, we propose ANTIPASTI, a convolutional neural network model that achieves state-of-the-art performance in the prediction of antibody binding affinity using as input a representation of antibody-antigen structures in terms of normal mode correlation maps derived from elastic network models. This representation captures not only structural features but energetic patterns of local and global residue fluctuations. The learnt representations are interpretable: they reveal similarities of binding patterns among antibodies targeting the same antigen type, and can be used to quantify the importance of antibody regions contributing to binding affinity. Our results show the importance of the antigen imprint in the normal mode landscape, and the dominance of cooperative effects and long-range correlations between antibody regions to determine binding affinity.
抗体对其同源靶标的高结合亲和力是引发有效免疫反应以及将抗体用作研究和治疗工具的关键。在此,我们提出了ANTIPASTI,这是一种卷积神经网络模型,它在使用基于弹性网络模型导出的正常模式相关图表示的抗体 - 抗原结构作为输入来预测抗体结合亲和力方面达到了当前的先进性能。这种表示不仅捕获了结构特征,还捕获了局部和全局残基波动的能量模式。所学习的表示是可解释的:它们揭示了靶向相同抗原类型的抗体之间结合模式的相似性,并且可用于量化抗体区域对结合亲和力贡献的重要性。我们的结果表明了正常模式景观中抗原印记的重要性,以及抗体区域之间协同效应和长程相关性对确定结合亲和力的主导作用。