Wang Yiquan, Lv Huibin, Lei Ruipeng, Yeung Yuen-Hei, Shen Ivana R, Choi Danbi, Teo Qi Wen, Tan Timothy J C, Gopal Akshita B, Chen Xin, Graham Claire S, Wu Nicholas C
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.
bioRxiv. 2023 Sep 14:2023.09.11.557288. doi: 10.1101/2023.09.11.557288.
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 inaccessibility of datasets for model training. In this study, we curated a dataset of >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 captured key sequence motifs 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 antibody response to influenza virus, but also provides an invaluable resource for applying deep learning to antibody research.
尽管抗体研究已有数十年,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,精心策划了一个包含5000多种流感血凝素(HA)抗体的数据集,该数据集揭示了针对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,我们利用这个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捕捉到了HA茎部抗体的关键序列基序。此外,通过将mBLM应用于具有未知表位的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抗体对流感病毒反应的分子理解,还为将深度学习应用于抗体研究提供了宝贵资源。