用结构检索增强扩散模型,让抗体设计更自然高效
Retrieval Augmented Diffusion Model for Structure-informed Antibody Design and Optimization
- 基于结构同源片段检索,引导抗体逆向折叠生成
- 在多个任务中达到当前最优性能,生成序列更自然
- 适用于各类生成模型,适合抗体药物研发人员
抗体是生物体免疫应答中的关键蛋白,可特异性识别病原体抗原。近年来生成模型显著推动了理性抗体设计的发展。但现有方法多从头生成抗体,缺乏模板约束,导致优化困难且序列不自然。为此,我们提出一种检索增强的扩散框架RADAb,用于高效抗体设计。该方法利用与查询结构约束匹配的结构同源片段,引导生成模型根据目标设计标准逆向优化抗体。具体而言,引入结构感知检索机制,通过新颖的双分支去噪模块将示范片段与输入骨架结合,同时利用结构和进化信息。此外,构建条件扩散模型,通过融合全局上下文和局部进化条件,迭代优化生成过程。本方法对生成模型选择无依赖性。实验证明,其在多个抗体逆折叠与优化任务中达到当前最优表现,为生物分子生成模型提供新思路。
原文摘要 · Abstract (English)
Antibodies are essential proteins responsible for immune responses in organisms, capable of specifically recognizing antigen molecules of pathogens. Recent advances in generative models have significantly enhanced rational antibody design. However, existing methods mainly create antibodies from scratch without template constraints, leading to model optimization challenges and unnatural sequences. To address these issues, we propose a retrieval-augmented diffusion framework, termed RADAb, for efficient antibody design. Our method leverages a set of structural homologous motifs that align with query structural constraints to guide the generative model in inversely optimizing antibodies according to desired design criteria. Specifically, we introduce a structure-informed retrieval mechanism that integrates these exemplar motifs with the input backbone through a novel dual-branch denoising module, utilizing both structural and evolutionary information. Additionally, we develop a conditional diffusion model that iteratively refines the optimization process by incorporating both global context and local evolutionary conditions. Our approach is agnostic to the choice of generative models. Empirical experiments demonstrate that our method achieves state-of-the-art performance in multiple antibody inverse folding and optimization tasks, offering a new perspective on biomolecular generative models.
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