鉴定关键磷酸化位点增强激酶活性与双峰融合框架。

IF 6.1 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS Molecular & Cellular Proteomics Pub Date : 2025-01-01 Epub Date: 2024-11-30 DOI:10.1016/j.mcpro.2024.100889
Menghuan Zhang, Yizhi Zhang, Keqin Dong, Jin Lin, Xingang Cui, Yong Zhang
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引用次数: 0

摘要

磷酸化是细胞中不可或缺的调节机制,激酶上的特定位点可以显著增强其活性。虽然几个这样的关键磷酸化位点(phos-sites)已经被实验确定,但更多的仍有待探索。到目前为止,还没有一种计算方法可以系统地识别这些激酶上的关键磷位点。在本研究中,我们介绍了PhoSiteformer,这是一个受变压器启发的基础模型,旨在使用磷酸化质谱(phos-MS)数据生成phos位点的嵌入。认识到蛋白质序列数据和phos-MS数据提供的互补见解,我们开发了一个采用双峰融合策略的分类模型CSPred。CSPred将来自PhoSiteformer的嵌入与来自蛋白质语言模型ProtT5的嵌入结合起来。我们的方法成功地鉴定了58个人类激酶的77个关键phos位点。其中两个位点,PRKG1上的T517和PRKD3上的T735,已经得到实验验证。这项研究提出了第一个系统的和计算的方法来确定关键的磷位点,增强激酶活性。
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Identification of Critical Phosphorylation Sites Enhancing Kinase Activity With a Bimodal Fusion Framework.

Phosphorylation is an indispensable regulatory mechanism in cells, with specific sites on kinases that can significantly enhance their activity. Although several such critical phosphorylation sites (phos-sites) have been experimentally identified, many more remain to be explored. To date, no computational method exists to systematically identify these critical phos-sites on kinases. In this study, we introduce PhoSiteformer, a transformer-inspired foundational model designed to generate embeddings of phos-sites using phosphorylation mass spectrometry data. Recognizing the complementary insights offered by protein sequence data and phosphorylation mass spectrometry data, we developed a classification model, CSPred, which employs a bimodal fusion strategy. CSPred combines embeddings from PhoSiteformer with those from the protein language model ProtT5. Our approach successfully identified 77 critical phos-sites on 58 human kinases. Two of these sites, T517 on PKG1 and T735 on PRKD3, have been experimentally verified. This study presents the first systematic and computational approach to identify critical phos-sites that enhance kinase activity.

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来源期刊
Molecular & Cellular Proteomics
Molecular & Cellular Proteomics 生物-生化研究方法
CiteScore
11.50
自引率
4.30%
发文量
131
审稿时长
84 days
期刊介绍: The mission of MCP is to foster the development and applications of proteomics in both basic and translational research. MCP will publish manuscripts that report significant new biological or clinical discoveries underpinned by proteomic observations across all kingdoms of life. Manuscripts must define the biological roles played by the proteins investigated or their mechanisms of action. The journal also emphasizes articles that describe innovative new computational methods and technological advancements that will enable future discoveries. Manuscripts describing such approaches do not have to include a solution to a biological problem, but must demonstrate that the technology works as described, is reproducible and is appropriate to uncover yet unknown protein/proteome function or properties using relevant model systems or publicly available data. Scope: -Fundamental studies in biology, including integrative "omics" studies, that provide mechanistic insights -Novel experimental and computational technologies -Proteogenomic data integration and analysis that enable greater understanding of physiology and disease processes -Pathway and network analyses of signaling that focus on the roles of post-translational modifications -Studies of proteome dynamics and quality controls, and their roles in disease -Studies of evolutionary processes effecting proteome dynamics, quality and regulation -Chemical proteomics, including mechanisms of drug action -Proteomics of the immune system and antigen presentation/recognition -Microbiome proteomics, host-microbe and host-pathogen interactions, and their roles in health and disease -Clinical and translational studies of human diseases -Metabolomics to understand functional connections between genes, proteins and phenotypes
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