Deep generative optimization of mRNA codon sequences for enhanced mRNA translation and therapeutic efficacy

Messenger RNA (mRNA) therapeutics show immense promise, but their efficacy is limited by suboptimal protein expression. Here, we present RiboDecode, a deep learning framework that generates mRNA codon sequences for enhanced mRNA translation. RiboDecode introduces several advances, including direct learning from large-scale ribosome profiling data and generative exploration of a large sequence space. In silico analysis demonstrates RiboDecode's robust predictive accuracy for unseen genes and cellular environments. In vitro experiments showed substantial improvements in protein expression, significantly outperforming past methods. In addition, RiboDecode enables mRNA design with consideration of cellular context and demonstrates robust performance across different mRNA formats, including m<sup>1</sup>Ψ-modified and circular mRNAs, an important feature for mRNA therapeutics. In vivo mouse studies showed that optimized influenza hemagglutinin mRNAs induce ten times stronger neutralizing antibody responses against influenza virus compared to the unoptimized sequence. In an optic nerve crush model, optimized nerve growth factor mRNAs achieve equivalent neuroprotection of retinal ganglion cells at one-fifth the dose of the unoptimized sequence. Collectively, RiboDecode represents a paradigm shift from rule-based to a data-driven, context-aware approach for mRNA therapeutic applications, enabling the development of more potent and dose-efficient treatments.

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Publication Details

Journal
Nature Communications
Published
2025-11-12
DOI
https://doi.org/10.1038/s41467-025-64894-x
Citations
4
Primary Topic
RNA and protein synthesis mechanisms
Type
article
Field-Weighted Citation Impact
3.22

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article

Deep generative optimization of mRNA codon sequences for enhanced mRNA translation and therapeutic efficacy

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4 citations
Nature Communications
RNA and protein synthesis mechanisms
3.22
article

Deep generative optimization of mRNA codon sequences for enhanced mRNA translation and therapeutic efficacy

Caijun Sun, Yong Hu, Gao‐Feng Zha, Linping Wu, Hao Zhou, Changyou Zhan, Zirong Han, Fan Wang, Xin He, Zhi Xie, Jianxiang Deng, Yupeng Li, Tong Li, Yao He, Zhaoyu Hu, Lin‐Feng Chen, Jiaqi Yang, Zehua Tang, Wenbing Jiang
article en
4 citations

Abstract

Messenger RNA (mRNA) therapeutics show immense promise, but their efficacy is limited by suboptimal protein expression. Here, we present RiboDecode, a deep learning framework that generates mRNA codon sequences for enhanced mRNA translation. RiboDecode introduces several advances, including direct learning from large-scale ribosome profiling data and generative exploration of a large sequence space. In silico analysis demonstrates RiboDecode's robust predictive accuracy for unseen genes and cellular environments. In vitro experiments showed substantial improvements in protein expression, significantly outperforming past methods. In addition, RiboDecode enables mRNA design with consideration of cellular context and demonstrates robust performance across different mRNA formats, including m<sup>1</sup>Ψ-modified and circular mRNAs, an important feature for mRNA therapeutics. In vivo mouse studies showed that optimized influenza hemagglutinin mRNAs induce ten times stronger neutralizing antibody responses against influenza virus compared to the unoptimized sequence. In an optic nerve crush model, optimized nerve growth factor mRNAs achieve equivalent neuroprotection of retinal ganglion cells at one-fifth the dose of the unoptimized sequence. Collectively, RiboDecode represents a paradigm shift from rule-based to a data-driven, context-aware approach for mRNA therapeutic applications, enabling the development of more potent and dose-efficient treatments.

Nature CommunicationsVol. 16(1)
Sun Yat-sen University (CN), Shenzhen University (CN), Fudan University (CN), Guangzhou Institutes of Biomedicine and Health (CN), The Seventh Affiliated Hospital of Sun Yat-sen University (CN), Beike Biotechnology (China) (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 7%
RNA and protein synthesis mechanisms
3.22
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