Evidence map›Paper›PMID 42265268›Full record

ArticleScientific reports2026

Enhancing the detection of LTP through lyophilized protein samples and NIR spectroscopy with explainable deep learning.

Ainhoa Osa-Sanchez, Itxasne Del Barrio, Ganeko Bernardo-Seisdedos, Sara Pozo, Begonya Garcia-Zapirain

Abstract read
In one paragraph

Article in Scientific reports, 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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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Ainhoa Osa-SanchezeVIDA Research Group, University of Deusto, Bilbao, 48007, Spain. ainhoa.osa.sanchez@deusto.es.
Itxasne Del BarrioeVIDA Research Group, University of Deusto, Bilbao, 48007, Spain.
Ganeko Bernardo-SeisdedosDeustoMED Research Group, University of Deusto, Bilbao, 48007, Spain.
Sara PozoDeustoMED Research Group, University of Deusto, Bilbao, 48007, Spain.
Begonya Garcia-ZapiraineVIDA Research Group, University of Deusto, Bilbao, 48007, Spain.

Funding

Eusko Jaurlaritza ZL-2025/00598
6 · The paper itself

Abstract

Lipid transfer proteins (LTPs) are clinically relevant allergens widely present in plant-based foods, and their reliable detection in complex food matrices remains a major challenge. In this study, we developed an integrated framework combining near-infrared spectroscopy (NIRS), deep learning, and explainability methods to enable accurate and interpretable identification of LTPs. A total of 11,688 spectral measurements were collect ed using a FLAME-NIR spectrometer (940-1700 nm) from homogenized food samples, purified Pru p 3 and Ara h 9 proteins, and their mixtures with LTP-free matrices such as yogurt and powdered milk. Spectral preprocessing involved first derivative transformation, Standard Normal Variate correction, and feature scaling, followed by dimensionality reduction through a 1D convolutional autoencoder, which generated 64-dimensional latent embeddings. These representations were used to train two deep learning classifiers Convolutional Neural Networks (CNNs) and TabTransformer optimized via Bayesian optimization. The inclusion of purified protein embeddings substantially improved classification performance. The CNN model achieved the highest performance with 95.8% accuracy, 97.3% precision, 96.9% F1-score, and an AUC-ROC of 0.954, outperforming the TabTransformer, which nonetheless reached 95.19% accuracy and 96.4% F1-score. Model explainability was addressed using SHAP and LIME, which identified key latent features corresponding to specific spectral regions (940-1700 nm) associated with allergenic signatures. Compared to baseline models, the protein-enhanced framework demonstrated marked improvements in specificity and overall robustness. These results highlight the value of incorporating purified protein information into AI-based spectral analysis, offering a portable, non-destructive, and interpretable strategy for allergen detection in food safety applications.

Indexed as

AllergensAntigens, PlantCarrier ProteinsDeep LearningPlant ProteinsAnimalsAutoencoderConvolutional Neural NetworksFreeze DryingSpectroscopy, Near-InfraredAllergensAntigens, PlantCarrier Proteinslipid transfer proteins, plantPlant ProteinsAllergensArtificial intelligenceClassificationExplainable artificial intelligenceLyophilizationNear-infrared spectroscopy

Identifiers

PMID42265268
PMCPMC13494038

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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.