Skip to content
DraconiticResearch
Search Sources API
197,768 studies31 sourcesUpdated 44 min ago
Peer-reviewedCC BYFrontiers in molecular biosciences

AIPFusion-Net: an interaction-fusion framework for anti-inflammatory peptide prediction using protein language model embeddings, local sequence patterns, and handcrafted descriptors.

  1. 1Department of Urology, Affiliated Hospital of Hebei University, Baoding, Hebei, China.
  2. 2Department of Emergency, Affiliated Hospital of Hebei University, Baoding, Hebei, China.

Abstract

Introduction

Anti-inflammatory peptides (AIPs) are promising candidates for treating inflammatory diseases. However, experimental identification is time-consuming and costly, creating a need for accurate computational prediction methods.Methods

We developed AIPFusion-Net, an interaction-fusion framework that integrates three complementary sources of peptide information: global contextual embeddings generated by the ESM2 protein language model, local sequence patterns extracted from biologically relevant subsequences, and handcrafted physicochemical and sequence descriptors. These representations were integrated through an interaction-fusion module and evaluated on two independent test datasets, Ind-1049 and Ind-426.Results

On the Ind-1049 dataset, AIPFusion-Net achieved an accuracy of 84.6%, sensitivity of 71.7%, specificity of 89.3%, MCC of 0.654, and AUC of 0.884. On the Ind-426 dataset, it achieved an accuracy of 82.3%, sensitivity of 84.4%, specificity of 76.9%, MCC of 0.673, and AUC of 0.882. The model outperformed the comparative predictors in overall classification performance and discriminative ability.Discussion

The results indicate that combining global contextual information, local sequence patterns, and handcrafted descriptors through interaction fusion improves the representation and identification of AIPs. AIPFusion-Net provides a useful computational framework for AIP screening and may support the discovery and design of novel anti-inflammatory peptides.

Related

  1. Representation learning for low-data protein fitness prediction using sequence–structure embeddings and graph neural networks
    Chanoknun Phunnasorn, Narupat Hongdilokkul, Wasakorn Laesanklang +2
    Scientific ReportsPeer-reviewedCC BY-NC-ND 4.0Full textMolecular biology & gene regulationCrossref
  2. Deciphering the Immune–Bone Interaction Network in Diabetic Bone Fragility: Inflammatory Mechanisms and Precision Therapeutics
    Wei Wang, Wei Xiong, Zheng Zhang
    BiomoleculesPeer-reviewedCC BY 4.0Molecular biology & gene regulationCrossref
  3. DeepEnzyKat: Turnover number prediction through enzyme-substrate interaction modeling and adaptive expert ensembles
    Guangran Zhang, Yujing Zhao, Yongwen Zhang +6
    ChemRxivPreprintCC BYMolecular biology & gene regulationChemRxiv
  4. Establishing standardized evaluation protocols for peptide-target interaction prediction: the PTI-TAPE consensus framework eDelphi
    William J. Waldock, Guangshun Wang, Ara Darzi +2
    Frontiers in bioinformaticsPeer-reviewedCC BYFull textMolecular biology & gene regulationEurope PMC
  5. A novel matrix multiplication framework for modeling genotype-by-environment interaction in genomic prediction
    Osval A. Montesinos-López, Abelardo Montesinos-López, Cricelio Montesinos-Lopez +5
    Frontiers in geneticsPeer-reviewedCC BYFull textGeneral biochemistryEurope PMC
BibTeX
@article{wang2026aipfusionnet,
  title = {{AIPFusion-Net: an interaction-fusion framework for anti-inflammatory peptide prediction using protein language model embeddings, local sequence patterns, and handcrafted descriptors.}},
  author = {Wentao Wang and Weidong Yang and Hongmei Li and Zhenyu Cui and Dan Shen},
  journal = {Frontiers in molecular biosciences},
  year = {2026},
  month = oct,
  doi = {10.3389/fmolb.2026.1952395},
  url = {https://europepmc.org/article/MED/42898259},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - AIPFusion-Net: an interaction-fusion framework for anti-inflammatory peptide prediction using protein language model embeddings, local sequence patterns, and handcrafted descriptors.
AU  - Wentao Wang
AU  - Weidong Yang
AU  - Hongmei Li
AU  - Zhenyu Cui
AU  - Dan Shen
PY  - 2026
DA  - 2026/10/05
JO  - Frontiers in molecular biosciences
DO  - 10.3389/fmolb.2026.1952395
UR  - https://europepmc.org/article/MED/42898259
AB  - Introduction  Anti-inflammatory peptides (AIPs) are promising candidates for treating inflammatory diseases. However, experimental identification is time-consuming and costly, creating a need for accurate computational prediction methods.Methods  We developed AIPFusion-Net, an interaction-fusion framework that integrates three complementary sources of peptide information: global contextual embeddings generated by the ESM2 protein language model, local sequence patterns extracted from biologically relevant subsequences, and handcrafted physicochemical and sequence descriptors. These representations were integrated through an interaction-fusion module and evaluated on two independent test datasets, Ind-1049 and Ind-426.Results  On the Ind-1049 dataset, AIPFusion-Net achieved an accuracy of 84.6%, sensitivity of 71.7%, specificity of 89.3%, MCC of 0.654, and AUC of 0.884. On the Ind-426 dataset, it achieved an accuracy of 82.3%, sensitivity of 84.4%, specificity of 76.9%, MCC of 0.673, and AUC of 0.882. The model outperformed the comparative predictors in overall classification performance and discriminative ability.Discussion  The results indicate that combining global contextual information, local sequence patterns, and handcrafted descriptors through interaction fusion improves the representation and identification of AIPs. AIPFusion-Net provides a useful computational framework for AIP screening and may support the discovery and design of novel anti-inflammatory peptides.
SN  - 2296-889X
ER  -