Evidence map›Paper›PMID 40235638›Full record

ArticleComputational and structural biotechnology journal2025

iNClassSec-ESM: Discovering potential non-classical secreted proteins through a novel protein language model.

Yizhou Shao, Taigang Liu

Abstract read
In one paragraph

Article in Computational and structural biotechnology journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Yizhou ShaoCollege of Information Technology, Shanghai Ocean University, Shanghai, 201306, China.
Taigang LiuCollege of Information Technology, Shanghai Ocean University, Shanghai, 201306, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-classical secreted proteins (NCSPs) are a class of proteins lacking signal peptides, secreted by Gram-positive bacteria through non-classical secretion pathways. With the increasing demand for highly secreted proteins in recent years, non-classical secretion pathways have received more attention due to their advantages over classical secretion pathways (Sec/Tat). However, because the mechanisms of non-classical secretion pathways are not yet clear, identifying NCSPs through biological experiments is expensive and time-consuming, making it imperative to develop computational methods to address this issue. Existing NCSP prediction methods mainly use traditional handcrafted features to represent proteins from sequence information, which limits the models' ability to capture complex protein characteristics. In this study, we proposed a novel NCSP predictor, iNClassSec-ESM, which combined deep learning with traditional classifiers to enhance prediction performance. iNClassSec-ESM integrates an XGBoost model trained on comprehensive handcrafted features and a Deep Neural Network (DNN) trained on hidden layer embeddings from the protein language model (PLM) ESM3. The ESM3 is the recently proposed multimodal PLM and has not yet been fully explored in terms of protein representation. Therefore, we extracted hidden layer embeddings from ESM3 as inputs for multiple classifiers and deep learning networks, and compared them with existing PLMs. Benchmark experiments indicate that iNClassSec-ESM outperforms most of existing methods across multiple performance metrics and could serve as an effective tool for discovering potential NCSPs. Additionally, the ESM3 hidden layer embeddings, as an innovative protein representation method, show great potential for the application in broader protein-related classification tasks. The source code of iNClassSec-ESM and the ESM3 embeddings extraction script are publicly available at https://github.com/AmamiyaHoshie/iNClassSec-ESM/.

Indexed as

EmbeddingsEnsemble learningNon-classical secreted proteinProtein language modelProtein representation

Identifiers

PMID40235638
PMCPMC11999076

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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.