论文标题

纳入抗体序列结构共设计的预训练范例

Incorporating Pre-training Paradigm for Antibody Sequence-Structure Co-design

论文作者

Gao, Kaiyuan, Wu, Lijun, Zhu, Jinhua, Peng, Tianbo, Xia, Yingce, He, Liang, Xie, Shufang, Qin, Tao, Liu, Haiguang, He, Kun, Liu, Tie-Yan

论文摘要

抗体是多功能蛋白,可以与病原体结合并为人体提供有效的保护。最近,基于深度学习的计算抗体设计引起了人们的关注,因为它自动从数据中自动挖掘抗体模式,这些模式可以与人类体验互补。但是,计算方法在很大程度上依赖于高质量的抗体结构数据,这是非常有限的。此外,互补性确定的区域(CDR)是确定特异性和结合亲和力的抗体的关键组成部分,是高度可变且难以预测的。因此,数据限制问题进一步增加了CDR生成抗体的困难。幸运的是,存在大量抗体的序列数据,可以帮助建模CDR并减轻对结构数据的依赖。通过见证蛋白质建模的预训练模型的成功,在本文中,我们开发了抗体预训练语言模型,并以系统的方式将其纳入(抗原特异性)抗体设计模型中。具体而言,我们首先根据序列数据预先进行抗体语言模型,然后为CDR的序列和结构生成序列和结构生成,以避免自动回归方式的沉重成本和误差传播,最后利用一些精心设计的模块来利用预训练的抗体抗体模型。通过各种实验,我们表明我们的方法在不同任务(例如序列和结构产生以及抗原结合CDR-H3设计)上实现了优于先前基线的表现。

Antibodies are versatile proteins that can bind to pathogens and provide effective protection for human body. 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 data limitation issue further raises the difficulty of CDR generation for antibodies. Fortunately, there exists a large amount of sequence data of antibodies that can help model the CDR and alleviate the 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 an antibody language model based on the sequence data, then propose a one-shot way for sequence and structure generation of CDR to avoid the heavy cost and error propagation from an autoregressive manner, and finally leverage the pre-trained antibody model for the antigen-specific antibody generation model with some carefully designed modules. Through various experiments, we show that our method achieves superior performances over previous baselines on different tasks, such as sequence and structure generation and antigen-binding CDR-H3 design.

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