AVP-GPT2: A Transformer-Powered Platform for De Novo Generation, Screening, and Explanation of Antiviral Peptides

Human respiratory syncytial virus (RSV) remains a significant global health threat, particularly for vulnerable populations. Despite extensive research, effective antiviral therapies are still limited. To address this urgent need, we present AVP-GPT2, a deep-learning model that significantly outperforms its predecessor, AVP-GPT, in designing and screening antiviral peptides. Trained on a significantly expanded dataset, AVP-GPT2 employs a transformer-based architecture to generate diverse peptide sequences. A multi-modal screening approach, incorporating Star-Transformer and Vision Transformer, enables accurate prediction of antiviral activity and toxicity, leading to the identification of potent and safe candidates. SHAP analysis further enhances interpretability by explaining the underlying mechanisms of peptide activity. Our in vitro experiments confirmed the antiviral efficacy of peptides generated by AVP-GPT2, with some exhibiting EC50 values as low as 0.01 μM and CC50 values > 30 μM. This represents a substantial improvement over AVP-GPT and traditional methods. AVP-GPT2 has the potential to significantly impact antiviral drug discovery by accelerating the identification of novel therapeutic agents. Future research will explore its application to other viral targets and its integration into existing drug development pipelines.

Authors

Publication Details

Journal
Viruses
Published
2024-12-25
DOI
https://doi.org/10.3390/v17010014
Citations
5
Primary Topic
Influenza Virus Research Studies
Type
article
Field-Weighted Citation Impact
1.93
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article

AVP-GPT2: A Transformer-Powered Platform for De Novo Generation, Screening, and Explanation of Antiviral Peptides

Huajian Zhao, Gengshen Song
5 citations
Viruses
Influenza Virus Research Studies
1.93
article

AVP-GPT2: A Transformer-Powered Platform for De Novo Generation, Screening, and Explanation of Antiviral Peptides

Huajian Zhao, Gengshen Song
article en
5 citations

Abstract

Human respiratory syncytial virus (RSV) remains a significant global health threat, particularly for vulnerable populations. Despite extensive research, effective antiviral therapies are still limited. To address this urgent need, we present AVP-GPT2, a deep-learning model that significantly outperforms its predecessor, AVP-GPT, in designing and screening antiviral peptides. Trained on a significantly expanded dataset, AVP-GPT2 employs a transformer-based architecture to generate diverse peptide sequences. A multi-modal screening approach, incorporating Star-Transformer and Vision Transformer, enables accurate prediction of antiviral activity and toxicity, leading to the identification of potent and safe candidates. SHAP analysis further enhances interpretability by explaining the underlying mechanisms of peptide activity. Our in vitro experiments confirmed the antiviral efficacy of peptides generated by AVP-GPT2, with some exhibiting EC50 values as low as 0.01 μM and CC50 values > 30 μM. This represents a substantial improvement over AVP-GPT and traditional methods. AVP-GPT2 has the potential to significantly impact antiviral drug discovery by accelerating the identification of novel therapeutic agents. Future research will explore its application to other viral targets and its integration into existing drug development pipelines.

VirusesVol. 17(1)
Good health and well-being
Openalex Percentile: Top 12%
Influenza Virus Research Studies
1.93
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