计算机科学
强化学习
人工智能
蛋白质设计
机器学习
水准点(测量)
谈判
理论(学习稳定性)
折叠(DSP实现)
蛋白质折叠
航程(航空)
进化算法
忠诚
多智能体系统
蛋白质结构预测
蛋白质工程
稳健性(进化)
作者
Mingming Zhu,Jiahua Rao,Dan Yang,Qianmu Yuan,Yuedong Yang
标识
DOI:10.64898/2026.01.13.699365
摘要
Abstract Protein design is revolutionizing biotechnology, yet existing approaches struggle to balance structural foldability with functional performance. Structure-based models excel at generating stable protein backbones but often overlook critical functional properties, while protein language models capture evolutionary and functional signals but frequently predict sequences lacking structural stability. Integrating these complementary approaches remains challenging due to their inherently conflicting objectives. We present MAProt, a multiagent framework that synergistically combines structure-based and protein language model-based methods for protein design. Each agent specializes in a distinct aspect of the design objective: the structure-based agent (e.g., ProteinMPNN) ensures compatibility with the target backbone, while protein language model-based agents (e.g., ESM, SaProt) capture evolutionary plausibility and functional potential. To reconcile conflicts and achieve optimal trade-offs, we introduce a Pareto-based negotiation module that enables effective multi-objective coordination and consensus among agents. Extensive experiments on benchmark datasets demonstrate that MAProt achieves a remarkable improvement over state-of-the-art baselines, and generalizes robustly across a range of tasks, including thermodynamic folding stability design, functional protein design, and high-affinity antibody design. These results highlight the power of collaborative optimization for advancing rational protein engineering. Code https://github.com/biomed-AI/MAProt
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