Evidence map›Paper›PMID 42737260›Full record

ArticleFoods (Basel, Switzerland)2026

iBitter-HF: A Method for Bitter Peptide Sequence Identification Based on Hybrid Feature Embedding.

Feng Yan, Shicheng Xiang, Yi Tang, Zhengran Kuang, Hengxi Liu, Ximei Luo, Zhibin Lv

Abstract read
In one paragraph

Article in Foods (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Feng YanCollege of Biomedical Engineering, Sichuan University, Chengdu 610041, China.
Shicheng XiangCollege of Biomedical Engineering, Sichuan University, Chengdu 610041, China.
Yi TangCollege of Biomedical Engineering, Sichuan University, Chengdu 610041, China.
Zhengran KuangCollege of Biomedical Engineering, Sichuan University, Chengdu 610041, China.
Hengxi LiuCollege of Biomedical Engineering, Sichuan University, Chengdu 610041, China.
Ximei LuoInstitute of Fundamental and Frontier Sciences, University of Electronic Science and Technology, Chengdu 610106, China.
Zhibin LvCollege of Biomedical Engineering, Sichuan University, Chengdu 610041, China.ORCID 0000-0001-5390-7616

Funding

National Natural Science Foundation of China 62371318
6 · The paper itself

Abstract

Bitter peptides are a practical barrier in food-grade protein hydrolysates, fermented products, and peptide-based supplements because they can compromise flavor before nutritional or functional value is realized. Sensory panels and mass-spectrometry-based identification remain reliable, but their throughput is limited for early screening of large peptide pools. Existing predictors usually emphasize either interpretable hand-crafted descriptors or deep sequence representations, whereas these two information sources may be complementary for food-oriented bitter peptide screening. Here, we propose iBitter-HF, a hybrid feature embedding method that integrates seven classes of hand-crafted descriptors with Unified Representation (UniRep) features. Light Gradient Boosting Machine (LGBM)-based feature-importance ranking was used to organize the candidate embeddings, and eXtreme Gradient Boosting (XGB) was used for classification of the selected feature subset. On the public BTP640 benchmark, the finalized 135-feature model achieved 96.9% accuracy on the independent test set. Literature-based comparison indicated competitive performance relative to eight reported bitter peptide predictors, and dimensionality reduction visualization suggested clearer local organization of bitter and non-bitter peptides after feature optimization. These results support iBitter-HF as a computational aid for sequence-level bitter peptide screening and debittering-oriented design of protein hydrolysates.

Indexed as

food protein hydrolysatesLightGBMpeptide bitternessphysicochemical descriptorsUniRepXGBoost

Identifiers

PMID42737260
PMCPMC13565165

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.