MetaDegron: multimodal feature-integrated protein language model for predicting E3 ligase targeted degrons

Protein degradation through the ubiquitin proteasome system at the spatial and temporal regulation is essential for many cellular processes. E3 ligases and degradation signals (degrons), the sequences they recognize in the target proteins, are key parts of the ubiquitin-mediated proteolysis, and their interactions determine the degradation specificity and maintain cellular homeostasis. To date, only a limited number of targeted degron instances have been identified, and their properties are not yet fully characterized. To tackle on this challenge, here we develop a novel deep-learning framework, namely MetaDegron, for predicting E3 ligase targeted degron by integrating the protein language model and comprehensive featurization strategies. Through extensive evaluations using benchmark datasets and comparison with existing method, such as Degpred, we demonstrate the superior performance of MetaDegron. Among functional features, MetaDegron allows batch prediction of targeted degrons of 21 E3 ligases, and provides functional annotations and visualization of multiple degron-related structural and physicochemical features. MetaDegron is freely available at http://modinfor.com/MetaDegron/. We anticipate that MetaDegron will serve as a useful tool for the clinical and translational community to elucidate the mechanisms of regulation of protein homeostasis, cancer research, and drug development.

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Publication Details

Journal
Briefings in Bioinformatics
Published
2024-09-23
DOI
https://doi.org/10.1093/bib/bbae519
Citations
7
Primary Topic
Protein Degradation and Inhibitors
Type
article
Field-Weighted Citation Impact
1.64

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article

MetaDegron: multimodal feature-integrated protein language model for predicting E3 ligase targeted degrons

Zhongming Zhao, Shaofeng Lin, Haodong Xu, Ruifeng Hu et al.
7 citations
Briefings in Bioinformatics
Protein Degradation and Inhibitors
1.64
article

MetaDegron: multimodal feature-integrated protein language model for predicting E3 ligase targeted degrons

Zhongming Zhao, Shaofeng Lin, Haodong Xu, Ruifeng Hu, Mengqiu Zheng, Kunqi Chen, Liming Wang
article en
7 citations

Abstract

Protein degradation through the ubiquitin proteasome system at the spatial and temporal regulation is essential for many cellular processes. E3 ligases and degradation signals (degrons), the sequences they recognize in the target proteins, are key parts of the ubiquitin-mediated proteolysis, and their interactions determine the degradation specificity and maintain cellular homeostasis. To date, only a limited number of targeted degron instances have been identified, and their properties are not yet fully characterized. To tackle on this challenge, here we develop a novel deep-learning framework, namely MetaDegron, for predicting E3 ligase targeted degron by integrating the protein language model and comprehensive featurization strategies. Through extensive evaluations using benchmark datasets and comparison with existing method, such as Degpred, we demonstrate the superior performance of MetaDegron. Among functional features, MetaDegron allows batch prediction of targeted degrons of 21 E3 ligases, and provides functional annotations and visualization of multiple degron-related structural and physicochemical features. MetaDegron is freely available at http://modinfor.com/MetaDegron/. We anticipate that MetaDegron will serve as a useful tool for the clinical and translational community to elucidate the mechanisms of regulation of protein homeostasis, cancer research, and drug development.

Briefings in BioinformaticsVol. 25(6)
Fujian Medical University (CN), The University of Texas MD Anderson Cancer Center (US), Central South University (CN), Hunan University (CN), Second Xiangya Hospital of Central South University (CN), The University of Texas Health Science Center at Houston (US)
National Natural Science Foundation of China, Fujian Medical University
Good health and well-being
Openalex Percentile: Top 16%
Protein Degradation and Inhibitors
1.64
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