Evidence map›Paper›PMID 39714581›Full record

ArticleInterdisciplinary sciences, computational life sciences2025

Identification of Multi-functional Therapeutic Peptides Based on Prototypical Supervised Contrastive Learning.

Sitong Niu, Henghui Fan, Fei Wang, Xiaomei Yang, Junfeng Xia

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Article in Interdisciplinary sciences, computational life sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

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5citing papers in PubMed
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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.

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3 · Its place in the literature

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5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Sitong NiuCollege of Mathematics and System sciences, Xinjiang University, Urumqi, 830046, Xinjiang, China.
Henghui FanInstitutes of Physical Science and Information Technology, Anhui University, Hefei, 230601, Anhui, China.
Fei WangSchool of Artificial Intelligence, Anhui University, Hefei, 230601, Anhui, China.
Xiaomei YangCollege of Mathematics and System sciences, Xinjiang University, Urumqi, 830046, Xinjiang, China. yxm_xju@126.com.ORCID http://orcid.org/0009-0007-2294-6103
Junfeng XiaInstitutes of Physical Science and Information Technology, Anhui University, Hefei, 230601, Anhui, China. jfxia@ahu.edu.cn.

Funding

Major Basic Research Project of the Natural Science Foundation of the Jiangsu Higher Education Institutions 2023AH051392the National Key Research and Development Program of China 2020YFA0908700the National Natural Science Foundation of China No.62362062Xinjiang Key Laboratory of Applied Mathematics XJDX1401
6 · The paper itself

Abstract

High-throughput sequencing has exponentially increased peptide sequences, necessitating a computational method to identify multi-functional therapeutic peptides (MFTP) from their sequences. However, existing computational methods are challenged by class imbalance, particularly in learning effective sequence representations. To address this, we propose PSCFA, a prototypical supervised contrastive learning with a feature augmentation method for MFTP prediction. We employ a two-stage training scheme to train the feature extractor and the classifier respectively, underpinned by the principle that better feature representation boosts classification accuracy. In the first stage, we utilize a prototypical supervised contrastive learning strategy to enhance the uniformity of feature space distribution, ensuring that the characteristics of samples within the same category are tightly clustered while those from different categories are more dispersed. In the second stage, a feature augmentation strategy that focuses on infrequent labels (tail labels) is used to refine the learning process of the classifier. We use a prototype-based variational autoencoder to capture semantic links among common labels (head labels) and their prototypes. This knowledge is then transferred to tail labels, generating enhanced features for classifier training. The experiments prove that the PSCFA method significantly outperforms existing methods for MFTP prediction, making a significant advancement in therapeutic peptide identification.

Indexed as

Computational BiologyPeptidesSupervised Machine LearningAlgorithmsHumansMachine LearningPeptidesContrastive learningFeature augmentationMulti-functional therapeutic peptide

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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.