NeoDesign: a computational tool for optimal selection of polyvalent neoantigen combinations

Abstract Motivation Tumor polyvalent neoantigen mRNA vaccines are gaining prominence in immunotherapy. The design of sequences in vaccine development is crucial for enhancing both the immunogenicity and safety of vaccines. However, a major challenge lies in selecting the optimal sequences from the l...

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Bibliographic Details
Published in:Bioinformatics (Oxford, England) Vol. 40; no. 10
Main Authors: Yu, Wenqian, Yu, Hongwu, Zhao, Jingjing, Zhang, Hena, Ke, Kalam, Hu, Zhixiang, Huang, Shenglin
Format: Journal Article
Language:English
Published: England Oxford University Press 01-10-2024
Oxford Publishing Limited (England)
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Summary:Abstract Motivation Tumor polyvalent neoantigen mRNA vaccines are gaining prominence in immunotherapy. The design of sequences in vaccine development is crucial for enhancing both the immunogenicity and safety of vaccines. However, a major challenge lies in selecting the optimal sequences from the large pools generated by multiple peptide combinations and synonymous codons. Results We introduce NeoDesign, a computational tool designed to tackle the challenge of sequence design. NeoDesign comprises four modules: Library Construction, Optimal Path Filtering, Linker Addition, and λ-Evaluation. It aims to identify the optimal protein sequence for tumor polyvalent neoantigen vaccines by minimizing linker usage, avoiding unexpected neoantigens and functional domains, and simplifying the structure. It also provides a preference scheme to balance mRNA stability and protein expression when designing mRNA sequences for the optimal protein sequence. This tool can potentially improve the sequence design of tumor polyvalent neoantigen mRNA vaccines, thereby significantly advancing immunotherapy strategies. Availability and implementation NeoDesign is freely available on https://github.com/HuangLab-Fudan/neoDesign and https://figshare.com/projects/NeoDesign/221704.
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ISSN:1367-4811
1367-4803
1367-4811
DOI:10.1093/bioinformatics/btae585