Wang Yiquan, Lv Huibin, Teo Qi Wen, Lei Ruipeng, Gopal Akshita B, Ouyang Wenhao O, Yeung Yuen-Hei, Tan Timothy J C, Choi Danbi, Shen Ivana R, Chen Xin, Graham Claire S, Wu Nicholas C
Department of Biochemistry, University of Illinois Urbana-Champaign, Urbana, IL 61801, USA.
Department of Biochemistry, University of Illinois Urbana-Champaign, Urbana, IL 61801, USA; Carl R. Woese Institute for Genomic Biology, University of Illinois Urbana-Champaign, Urbana, IL 61801, USA.
Immunity. 2024 Oct 8;57(10):2453-2465.e7. doi: 10.1016/j.immuni.2024.07.022. Epub 2024 Aug 19.
Despite decades of antibody research, it remains challenging to predict the specificity of an antibody solely based on its sequence. Two major obstacles are the lack of appropriate models and the inaccessibility of datasets for model training. In this study, we curated >5,000 influenza hemagglutinin (HA) antibodies by mining research publications and patents, which revealed many distinct sequence features between antibodies to HA head and stem domains. We then leveraged this dataset to develop a lightweight memory B cell language model (mBLM) for sequence-based antibody specificity prediction. Model explainability analysis showed that mBLM could identify key sequence features of HA stem antibodies. Additionally, by applying mBLM to HA antibodies with unknown epitopes, we discovered and experimentally validated many HA stem antibodies. Overall, this study not only advances our molecular understanding of the antibody response to the influenza virus but also provides a valuable resource for applying deep learning to antibody research.
尽管进行了数十年的抗体研究,但仅根据抗体序列预测其特异性仍然具有挑战性。两个主要障碍是缺乏合适的模型以及用于模型训练的数据集难以获取。在本研究中,我们通过挖掘研究出版物和专利精心挑选了5000多种流感血凝素(HA)抗体,这揭示了针对HA头部和茎部结构域的抗体之间许多不同的序列特征。然后,我们利用该数据集开发了一种轻量级记忆B细胞语言模型(mBLM),用于基于序列的抗体特异性预测。模型可解释性分析表明,mBLM可以识别HA茎部抗体的关键序列特征。此外,通过将mBLM应用于表位未知的HA抗体,我们发现并通过实验验证了许多HA茎部抗体。总体而言,本研究不仅推进了我们对流感病毒抗体反应的分子理解,还为将深度学习应用于抗体研究提供了宝贵资源。