Authors
Juseong Kim, Jeongmu Kim, Jae-Wook Lee, Qian Qi, Caroline Danehy, Ho Young Kang, Yong Cheng, Giltae Song
Published in
Molecular therapy. Nucleic acids. Volume 37. Issue 3. Pages 102991. Sep 08, 2026. Epub Jun 18, 2026.
Abstract
Following the success of COVID-19 vaccines and therapies, mRNA-based therapeutics have attracted significant attention. Codon optimization is crucial for improving translation efficiency and mRNA stability, both of which are necessary for developing effective mRNA vaccines and drugs. Traditional approaches often rely on codon usage tables and other frequency-based heuristics, which neglect sequence context and show limited scalability. We introduce COformer, a deep learning framework for codon optimization that captures codon-level features related to protein expression in Homo sapiens cells. By integrating convolutional neural networks (CNNs) and transformers, the model learns local and global sequence contexts influencing translation efficiency and stability, while contrastive learning aligns codon representations with amino acid identities. Trained on sequences optimized by commercial tools, COformer generates codon choices that, when validated in in vitro experiments, enhance protein expression through optimized codon usage and improved mRNA stability.
PMID:
42405277
Bibliographic data and abstract were imported from PubMed on 06 Jul 2026.
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