# Multi-AOP: a lightweight multi-view deep learning framework for antioxidant peptide discovery

**Authors:** Jianxiu Cai, Xinpo Lou, Chak Fong Chong, Deepa Alex, Joel P. Arrais, Yapeng Wang, Shirley W. I. Siu

PMC · DOI: 10.1186/s40643-025-01004-1 · Bioresources and Bioprocessing · 2026-02-02

## TL;DR

Multi-AOP is a new deep learning framework that improves the discovery of antioxidant peptides by combining sequence and molecular graph features.

## Contribution

Introduces a lightweight multi-view deep learning framework for AOP discovery that outperforms existing methods.

## Key findings

- Multi-AOP achieves high accuracy on benchmark datasets (0.8043, 0.9684, and 0.9043).
- Combining sequence and graph features improves AOP prediction performance.
- A unified AOP dataset was created to support future model development.

## Abstract

Antioxidant peptides (AOPs), with their strong free radical scavenging ability and health benefits, have emerged as promising candidates for disease prevention and food preservation. However, traditional experimental approaches to AOP discovery remain hindered by inefficiencies and substantial resource demands. Here, we present Multi-AOP, a parameter lightweight multi-view deep learning framework (0.75 million parameters) that enhances AOP discovery through integrated sequence and graph learning. We employ Extended Long Short-Term Memory (xLSTM) to generate sequence embeddings. Concurrently, we transform peptide sequences into SMILES representations and extract molecular graph features using a Message Passing Neural Network (MPNN), capturing intrinsic physicochemical properties. By leveraging both sequence patterns and structural information through hierarchical fusion, Multi-AOP achieves accuracies of 0.8043, 0.9684, and 0.9043 on the AnOxPePred, AnOxPP, and AOPP benchmark datasets, respectively, consistently outperforming conventional machine learning algorithms and state-of-the-art deep learning approaches. Furthermore, we constructed a unified AOP dataset by integrating these benchmark datasets, facilitating the future development of generalizable AOP models. All datasets and the optimized predictive model are publicly accessible at https://github.com/CaiJianxiu/Multi-AOP.

The online version contains supplementary material available at 10.1186/s40643-025-01004-1.

## Full-text entities

- **Diseases:** AOPs (MESH:C565529), MPNN (MESH:D015441), toxicity (MESH:D064420), DL (MESH:D007859), chronic diseases (MESH:D002908)
- **Chemicals:** AnOxPP (-), glutamine (MESH:D005973), amino acids (MESH:D000596), histidine (MESH:D006639), Acid (MESH:D000143), ROS (MESH:D017382)

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## Figures

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## References

8 references — full list in the complete paper: https://tomesphere.com/paper/PMC12864603/full.md

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Source: https://tomesphere.com/paper/PMC12864603