Evidence map›Paper›PMID 40518951›Full record

ArticleBriefings in bioinformatics2025

MultiPep-DLCL: recognition of multifunctional therapeutic peptides through deep learning with label-sequence contrastive learning.

Ting Li, Henghui Fan, Jianping Zhao, Xiaomei Yang, Junfeng Xia

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 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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

5 authors.

Ting LiCollege of Mathematics and Systems Science, Xinjiang University, No. 777 Huarui Road, Shuimogou District, Urumqi, Xinjiang Uygur Autonomous Region 830046, China.
Henghui FanInstitutes of Physical Science and Information Technology, Anhui University, No. 111 Jiulong Road, Economic and Technological Development Zone, Hefei, Anhui Province 230601, China.
Jianping ZhaoCollege of Mathematics and Systems Science, Xinjiang University, No. 777 Huarui Road, Shuimogou District, Urumqi, Xinjiang Uygur Autonomous Region 830046, China.
Xiaomei YangCollege of Mathematics and Systems Science, Xinjiang University, No. 777 Huarui Road, Shuimogou District, Urumqi, Xinjiang Uygur Autonomous Region 830046, China.
Junfeng XiaInstitutes of Physical Science and Information Technology, Anhui University, No. 111 Jiulong Road, Economic and Technological Development Zone, Hefei, Anhui Province 230601, China.

Funding

Anhui Higher Education Institutions of China 2023AH051392Multimodal Major Chronic Disease Prevention and Control Science and Engineering Research Project MCD-2023-1-15National Key Research and Development Program of China 2020YFA0908700National Natural Science Foundation of China 62362062"Tianshan Elite" Youth Talents-Youth Science and Technology Innovation Talents of the Autonomous Region 2023TSYCCX0104
6 · The paper itself

Abstract

Identifying multifunctional therapeutic peptides (MFTP) is an important yet complex challenge in the realm of peptide recognition. Unlike monofunctional peptides, MFTP classification requires discerning fine-grained labeling information associated with amino acids, making it more intricate. Existing methods often ignore the nuanced semantics of these labels and fail to fully explore the interplay between peptide sequences and their labels. To address these issues, we propose a multilabel classification method named MultiPep-DLCL. This method uses a deep learning-based model architecture to translate peptide sequences into sequence features by learning the local and global dependencies of multifunctional therapeutic peptide sequences. Additionally, the Label-Sequence Fusion Transformer is employed to efficiently learn high-quality label embeddings by mining effective information from peptide sequences. Finally, the correspondence between sequence features and label embeddings is strengthened through label-sequence contrastive learning. To tackle dataset imbalance, MultiPep-DLCL integrates a multilabel focal dice loss function alongside the traditional cross-entropy loss function. Experimental results demonstrate that the MultiPep-DLCL significantly outperforms existing methods in MFTP recognition.

Indexed as

Deep LearningPeptidesAlgorithmsAmino Acid SequenceHumansPeptidescontrastive learninglabel embeddingmultilabel classificationtherapeutic peptide recognition

Identifiers

PMID40518951
PMCPMC12167766

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.