Evidence map›Paper›PMID 41749211›Full record

ArticleBMC biology2026

BiToxNet: a deep learning framework integrating multimodal features for accurate identification of neurotoxic peptides and proteins.

Feng Wang, Peilin Xie, Xingqiao Lin, Jiahui Guan, Chang Liu, Xuxin He, Tzong-Yi Lee, Leyi Wei, Xiangrong Liu, Lantian Yao

Abstract read
In one paragraph

Article in BMC biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

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

10 authors.

Feng Wang *School of Informatics, Xiamen University, 361005, Xiamen, China.
Peilin Xie *Kobilka Institute of Innovative Drug Discovery, School of Medicine, The Chinese University of Hong Kong, Shenzhen, 2001 Longxiang Road, 518172, Shenzhen, China.
Xingqiao Lin *School of Medicine, The Chinese University of Hong Kong, Shenzhen, 2001 Longxiang Road, 518172, Shenzhen, China.
Jiahui GuanKobilka Institute of Innovative Drug Discovery, School of Medicine, The Chinese University of Hong Kong, Shenzhen, 2001 Longxiang Road, 518172, Shenzhen, China.
Chang LiuSchool of Medicine, The Chinese University of Hong Kong, Shenzhen, 2001 Longxiang Road, 518172, Shenzhen, China.
Xuxin HeSchool of Medicine, The Chinese University of Hong Kong, Shenzhen, 2001 Longxiang Road, 518172, Shenzhen, China.
Tzong-Yi LeeInstitute of Bioinformatics and Systems Biology, National Yang Ming Chiao Tung University, Hsinchu, Taiwan.
Leyi WeiFaculty of Applied Sciences, Macao Polytechnic University, R. de Luís Gonzaga Gomes, 999078, Macao, China. weileyi@sdu.edu.cn.
Xiangrong LiuSchool of Informatics, Xiamen University, 361005, Xiamen, China. xrliu@xmu.edu.cn.
Lantian YaoSchool of Informatics, Xiamen University, 361005, Xiamen, China. lantianyao@xmu.edu.cn.

Funding

Fundamental Research Funds for the Central Universities 20720250172National Science and Technology Council NSTC 113-2321-B-A49-025Shenzhen Science and Technology Innovation Commission JCYJ20230807114206014The National Health Research Institutes NHRI-EX114-11320BIYushan Young Fellow Program 113C51N055
6 · The paper itself

Abstract

backgroundAccurate prediction of the neurotoxicity of peptides and proteins is critically important for the safety assessment of protein therapeutics and the development of protein-based drugs. Although experimental methods can reliably identify neurotoxic peptides and neurotoxins, they are labor-intensive, costly, and unsuitable for large-scale screening. Existing computational approaches are often limited by shallow feature engineering and suboptimal multimodal fusion strategies, which restrict their predictive accuracy and generalizability in real-world applications.

resultsIn this study, we propose BiToxNet, a deep learning framework that integrates evolutionary embeddings derived from a protein large language model with ten handcrafted biochemical descriptors through a bilinear attention network (BAN). This design enables effective modeling of cross-modal interactions and residue-level dependencies critical for neurotoxicity prediction. BiToxNet was evaluated on three datasets of different sequence lengths, namely Protein, Peptide, and Combined datasets, achieving accuracies of 92.3%, 96.0%, and 92.7%, respectively, and consistently outperforming existing state-of-the-art methods. Ablation studies confirmed the importance of both evolutionary embeddings and handcrafted features, as well as the critical role of BAN in feature fusion. Visualization analyses using t-SNE and hierarchical clustering further demonstrated that BiToxNet learns highly discriminative representations without reliance on domain-specific prior knowledge. Additional evaluation on an external imbalanced dataset validated the robustness and strong generalization capability of the proposed framework.

conclusionsOverall, BiToxNet provides a powerful and generalizable computational framework for the accurate identification of neurotoxic peptides and proteins. By effectively integrating evolutionary and biochemical information through bilinear attention, BiToxNet offers a valuable tool for neurotoxin screening and protein drug safety assessment, and presents a distinctive modeling strategy applicable to a wide range of biological sequence analysis tasks.

Indexed as

Computational BiologyDeep LearningNeurotoxinsPeptidesProteinsAnimalsNeurotoxinsPeptidesProteinsBilinear attention networkDeep learningDrug discoveryNeurotoxinsSequence analysis

Identifiers

PMID41749211
PMCPMC13040786

What Socratic holds

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LicenceCC BY-NC-ND
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Registered trials

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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 Socratic graph.