Deep Learning and Artificial Intelligence in the Design of Angiotensin-Converting Enzyme (ACE) Inhibitory Peptides

Main Article Content

Zhangheng Qian
Yunuo Zhou
Ruotong Lin
Yang Hong
Yunzhe Xu
Shipeng Li
Jiangcheng Gao
Qiurui Zhu
Heng Zheng

Abstract

Background: Hypertension is a major modifiable risk factor for cardiovascular disease (CVD), and angiotensin-converting enzyme (ACE) remains a principal target within the renin-angiotensin-aldosterone system (RAAS). Food-derived ACE inhibitory peptides (ACEiPs) are attractive because of their specificity and generally favorable safety profile, but conventional discovery through protein hydrolysis, fractionation, purification, and repeated activity assays is labor-intensive and samples only a small fraction of the possible sequence space. Scope and approach: Unlike reviews that consider databases, predictive models, generative methods, or structural validation as separate topics, this review organizes these components into an integrated closed-loop workflow. It connects curated ACEiP data, sequence and chemical encodings, machine-learning and deep-learning predictors, de novo generation, structure prediction, docking, molecular dynamics, free-energy estimation, experimental validation, and feedback-guided model refinement. Key findings and conclusions: The analysis shows that database heterogeneity, inconsistent IC50 assay conditions, class imbalance, and sequence redundancy can limit model generalization. For short food-derived peptides, simple composition and physicochemical descriptors remain competitive baselines; protein language models (PLMs) can add contextual information but may be affected by protein-to-peptide domain shift, whereas SMILES and self-referencing embedded strings (SELFIES) are most useful when atom-level connectivity, stereochemistry, or non-canonical residues must be represented. A practical post-screening stage should jointly assess potency, ACE-domain binding, gastrointestinal stability, permeability, solubility, toxicity, allergenicity, and manufacturability. Progress toward translation therefore depends on a closed loop in which experimentally measured activity and developability data update the training set and guide subsequent design cycles.

Article Details

Qian, Z., Zhou, Y., Lin, R., Hong, Y., Xu, Y., Li, S., … Zheng, H. (2026). Deep Learning and Artificial Intelligence in the Design of Angiotensin-Converting Enzyme (ACE) Inhibitory Peptides. Journal of Artificial Intelligence Research and Innovation, 83–96. https://doi.org/10.29328/journal.jairi.1001022
Review Articles

Copyright (c) 2026 Qian Z, et al.

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This work is licensed under a Creative Commons Attribution 4.0 International License.

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