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ArticleInterdisciplinary sciences, computational life sciences2026

MBPBERT: A Large Language Model for Metal-Binding Peptide Discovery.

Guifen Jian, Xinwei Li, Yu Chen, Junjie Liu, Ziyang Liu, Xing Shang, Heng Chen, Jian Huang, Bifang He

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Article in Interdisciplinary sciences, computational life sciences, 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

9 authors.

Guifen JianMedical College, Guizhou University, Guiyang, 550025, China.
Xinwei LiMedical College, Guizhou University, Guiyang, 550025, China.
Yu ChenMedical College, Guizhou University, Guiyang, 550025, China.
Junjie LiuMedical College, Guizhou University, Guiyang, 550025, China.
Ziyang LiuMedical College, Guizhou University, Guiyang, 550025, China.
Xing ShangMedical College, Guizhou University, Guiyang, 550025, China.
Heng ChenMedical College, Guizhou University, Guiyang, 550025, China. hchen13@gzu.edu.cn.
Jian HuangSchool of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu, 611731, China. hj@uestc.edu.cn.
Bifang HeMedical College, Guizhou University, Guiyang, 550025, China. bfhe@gzu.edu.cn.

Funding

Guizhou Provincial Science and Technology Department MS[2026]144Guizhou Provincial Science and Technology Department MS[2026]145Health Commission of Guizhou Province gzwkj2025-043Health Commission of Guizhou Province gzwkj2025-141National Natural Science Foundation of China 62261006National Natural Science Foundation of China 62263003National Natural Science Foundation of China 82360340
6 · The paper itself

Abstract

Metal-binding peptides (MBPs) are a class of peptides capable of selectively coordinating metal ions and play critical roles in various biological processes, such as metal ion transport, storage, catalysis, and signal transduction. However, traditional experimental approaches, such as mass spectrometry, chromatography, and nuclear magnetic resonance spectroscopy, are labor-intensive, time-consuming, and poorly suited for the large-scale screening of MBPs. To overcome these limitations, we introduce MBPBERT, a deep learning-based predictive framework for accurate identification of MBPs and discrimination of metal-specific binding subtypes. MBPBERT builds upon the ProteinBERT architecture and was developed using two curated datasets: a peptide pretraining corpus comprising 33,095 sequences and a labeled dataset containing 909 MBPs and non-MBPs. For rigorous external validation, an independent test dataset of 101 peptides was constructed. MBPBERT attained areas under the receiver operating characteristic curve (AUROCs) of 0.9414 and 0.8882 on the test dataset for the prediction of MBPs and the classification of their specific binding subtypes, respectively. These results underscore the framework's strong predictive capability and generalization performance. Thus, MBPBERT provides a scalable and efficient in silico solution for high-throughput discovery of novel MBPs and screening of peptides with metal-specific binding preferences, potentially reducing the reliance on resource-intensive experimental validation.

Indexed as

In silico screeningMBPBERTMetal-binding peptide (MBP)ProteinBERT

Identifiers

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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.