Evidence map›Paper›PMID 40874821›Full record

ArticleBriefings in bioinformatics2025

ESM2_AMP: an interpretable framework for protein-protein interactions prediction and biological mechanism discovery.

Yawen Sun, Rui Wang, Zeyu Luo, Lejia Tan, Junhao Liu, Ruimeng Li, Dongqing Wei, Yu-Juan Zhang

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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.

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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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

8 authors.

Yawen SunCollege of Life Science, Chongqing Normal University, No. 37 University Town Road, high-tech District, Chongqing 401331, P.R. China.
Rui WangCollege of Life Science, Chongqing Normal University, No. 37 University Town Road, high-tech District, Chongqing 401331, P.R. China.
Zeyu LuoCollege of Life Science, Chongqing Normal University, No. 37 University Town Road, high-tech District, Chongqing 401331, P.R. China.ORCID 0000-0001-6650-9975
Lejia TanCollege of Life Science, Chongqing Normal University, No. 37 University Town Road, high-tech District, Chongqing 401331, P.R. China.
Junhao LiuCollege of Life Science, Chongqing Normal University, No. 37 University Town Road, high-tech District, Chongqing 401331, P.R. China.
Ruimeng LiCollege of Life Science, Chongqing Normal University, No. 37 University Town Road, high-tech District, Chongqing 401331, P.R. China.
Dongqing WeiState Key Laboratory of Microbial Metabolism, Joint International Research Laboratory of Metabolic & Developmental Sciences and School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, 800 Dongchuan RD. Minhang District, Shanghai 200030, P.R. China.ORCID 0000-0003-4200-7502
Yu-Juan ZhangCollege of Life Science, Chongqing Normal University, No. 37 University Town Road, high-tech District, Chongqing 401331, P.R. China.ORCID 0000-0001-6361-0840

Funding

National Natural Science Foundation of China 31871274Natural Science Foundation of Chongqing, China CSTB2022NSCQ-MSX0650
6 · The paper itself

Abstract

The prediction of binary protein-protein interactions (PPIs) is essential for protein engineering, but a major challenge in deep learning-based methods is the unknown decision-making process of the model. To address this challenge, we propose the ESM2_AMP framework, which utilizes the ESM2 protein language model for extracting segment features from actual amino acid sequences and integrates the Transformer model for feature fusion in binary PPIs prediction. Further, the two distinct models, ESM2_AMPS and ESM2_AMP_CSE are developed to systematically explore the contributions of segment features and combine with special tokens features in the decision-making process. The experimental results reveal that the model relying on segment features demonstrates strong correlations between segments with high attention weights and known functional regions of amino acid sequences. This insight suggests that attention to these segments helps capture biologically relevant functional and interaction-related information. By analyzing the coverage relationship between high-attention sequence fragments and functional regions, we validated the model's ability to capture key segment features of PPIs and revealed the critical role of functional domains in PPIs. This finding not only enhances the interpretability methods for sequence-based prediction models but also provides biological evidence supporting the important regulatory role of functional sequences in protein-protein interactions. It offers cross-disciplinary insights for algorithm optimization and experimental validation research in the field of computational biology.

Indexed as

Computational BiologyDeep LearningProtein Interaction MappingProteinsAlgorithmsAmino Acid SequenceDatabases, ProteinHumansSoftwareProteinsattention mechanismfunctional amino acid regioninterpretable analysisprotein–protein interaction

Identifiers

PMID40874821
PMCPMC12392411

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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.