<i>De Novo</i> Multi‐Mechanism Antimicrobial Peptide Design via Multimodal Deep Learning

Artificial intelligence (AI)-driven discovery of antimicrobial peptides (AMPs) is yet to fully utilize their three-dimensional (3D) structural characteristics, microbial species-specific antimicrobial activities, and mechanisms. Here, we constructed a QLAPD database comprising the sequence, structures, and antimicrobial properties of 12 914 AMPs. QLAPD underlies a multimodal, multitask, multilabel, and conditionally controlled AMP discovery (M3-CAD) pipeline, proposed for the de novo design of multi-mechanism AMPs to combat multidrug-resistant organisms (MDROs). This pipeline integrates generation, regression, and classification modules, using an innovative 3D voxel coloring method to capture the nuanced physicochemical context of amino acids, thus enhancing structural characterizations. QLX-3DV-1 and QLX-3DV-2, identified through M3-CAD, were found to demonstrate multiple antimicrobial mechanisms, notable activity against MDROs, and low toxicity. In vivo experiments were used to validate their antimicrobial effects with limited local and systemic toxicity. Overall, integrating 3D features, species-specific antimicrobial activities, and mechanisms enhanced AI-driven AMP discovery, making the M3-CAD pipeline a viable tool for de novo AMP design.

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Publication Details

Journal
Advanced Science
Published
2026-03-09
DOI
https://doi.org/10.1002/advs.202515835
Primary Topic
Antimicrobial Peptides and Activities
Type
article
Field-Weighted Citation Impact
0.00
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article

De Novo Multi‐Mechanism Antimicrobial Peptide Design via Multimodal Deep Learning

Xueping Nan, Xiaodong Li, Haifan Gong, Lei Li et al.
Advanced Science
Antimicrobial Peptides and Activities
article

De Novo Multi‐Mechanism Antimicrobial Peptide Design via Multimodal Deep Learning

Xueping Nan, Xiaodong Li, Haifan Gong, Lei Li, X-L Zuo, Peijing Bao, Zhongxue Han, Yuerui Ma, Boyao Wan, Yinuo Zhao, Jiekun Ni, Longfei Sun, Haina Wang, Qingzhou Kong, Xiaoyun Yang, Jialu Fu, Kunping Ju, Jinghui Zhang, Huijun Chang, Yanqing Li, Mengqi Zheng, Yanbo Yu, Yumeng Zhang, Yue Wang
article en

Abstract

Artificial intelligence (AI)-driven discovery of antimicrobial peptides (AMPs) is yet to fully utilize their three-dimensional (3D) structural characteristics, microbial species-specific antimicrobial activities, and mechanisms. Here, we constructed a QLAPD database comprising the sequence, structures, and antimicrobial properties of 12 914 AMPs. QLAPD underlies a multimodal, multitask, multilabel, and conditionally controlled AMP discovery (M3-CAD) pipeline, proposed for the de novo design of multi-mechanism AMPs to combat multidrug-resistant organisms (MDROs). This pipeline integrates generation, regression, and classification modules, using an innovative 3D voxel coloring method to capture the nuanced physicochemical context of amino acids, thus enhancing structural characterizations. QLX-3DV-1 and QLX-3DV-2, identified through M3-CAD, were found to demonstrate multiple antimicrobial mechanisms, notable activity against MDROs, and low toxicity. In vivo experiments were used to validate their antimicrobial effects with limited local and systemic toxicity. Overall, integrating 3D features, species-specific antimicrobial activities, and mechanisms enhanced AI-driven AMP discovery, making the M3-CAD pipeline a viable tool for de novo AMP design.

Advanced Science
Shandong University (CN), Shanghai Jiao Tong University (CN), Nanjing University of Science and Technology (CN), National Clinical Research Center for Digestive Diseases (CN), Shandong Provincial Hospital (CN), Chinese University of Hong Kong, Shenzhen (CN), Shandong Academy of Pharmaceutical Sciences (CN), Qilu Hospital of Shandong University (CN), Shandong Center for Disease Control and Prevention (CN)
Openalex Percentile: Top 30%
Antimicrobial Peptides and Activities
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