计算机科学
杠杆(统计)
抗体
互补决定区
语言模型
人工智能
免疫学
生物
单克隆抗体
作者
K. Y. Gao,Lijun Wu,Jinhua Zhu,Tian-Bo Peng,Yingce Xia,Liang He,Shufang Xie,Shufang Xie,Haiguang Liu,Kun He,Tie‐Yan Liu
标识
DOI:10.1145/3580305.3599468
摘要
Antibodies are proteins that effectively protect the human body by binding to pathogens. Recently, deep learning-based computational antibody design has attracted popular attention since it automatically mines the antibody patterns from data that could be complementary to human experiences. However, the computational methods heavily rely on high-quality antibody structure data, which is quite limited. Besides, the complementarity-determining region (CDR), which is the key component of an antibody that determines the specificity and binding affinity, is highly variable and hard to predict. Therefore, the limited availability of high-quality antibody structure data exacerbates the difficulty of CDR generation. Fortunately, there is a large amount of sequence data for antibodies that can help model the CDR and reduce reliance on structure data. By witnessing the success of pre-training models for protein modeling, in this paper, we develop the antibody pre-training language model and incorporate it into the antigen-specific antibody design model in a systemic way. Specifically, we first pre-train a novel antibody language model based on the sequence data, then propose a one-shot way for sequence and structure generation of CDR to mitigate the high cost and error propagation associated with autoregressive methods, and finally leverage the pre-trained antibody model for the antigen-specific antibody generation model with some carefully designed modules. Our experiments demonstrate the superiority of our method over previous baselines in tasks such as sequence and structure generation, CDR-H3 design for antigen binding, and antibody optimization1. The code is available at https://github.com/KyGao/ABGNN.
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