{"title":"Employing Expression-Matched Controls Enables High-Confidence Proximity-Based Interactome Classification.","authors":"Fulin Jiang, Xuezhen Ge, Eric J Bennett","doi":"10.1016/j.mcpro.2025.101001","DOIUrl":null,"url":null,"abstract":"<p><p>Proximity labeling approaches have been widely utilized to define protein interactomes. Due to the inherent promiscuity of proximity labeling using TurboID-based approaches, identification and adoption of appropriate labeling controls is a pivotal step to mitigate background interference and enhance interactome assignment accuracy. Here, we evaluate the effectiveness of both expression controls and data normalization strategies in generating high-confidence interactome maps. We demonstrate that the extent of control of TurboID protein expression is strongly correlated with overall signal intensity and the number of identified proteins from streptavidin-enrichments. Discordant expression levels between the bait and control samples result in high-frequency false-negative and false-positive identifications. Data normalization strategies help correct these expression differences but also introduce data distortion for proteins with high or low endogenous expression. Using the ubiquitin ligases RNF10 and HUWE1 as bait proteins, we demonstrate that matching TurboID expression between control and bait proteins allows for similar sampling of non-specific interactions. Using a matched expression strategy results in significantly reduced background interference and increases the accuracy of interactome assignments. These results document the need to alter proximity-labeling experimental workflows to include the generation of matched expression controls to enhance proximity labeling proteomics interactome mapping robustness and reproducibility.</p>","PeriodicalId":18712,"journal":{"name":"Molecular & Cellular Proteomics","volume":" ","pages":"101001"},"PeriodicalIF":5.5000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12226361/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular & Cellular Proteomics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.mcpro.2025.101001","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/5/27 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0
Abstract
Proximity labeling approaches have been widely utilized to define protein interactomes. Due to the inherent promiscuity of proximity labeling using TurboID-based approaches, identification and adoption of appropriate labeling controls is a pivotal step to mitigate background interference and enhance interactome assignment accuracy. Here, we evaluate the effectiveness of both expression controls and data normalization strategies in generating high-confidence interactome maps. We demonstrate that the extent of control of TurboID protein expression is strongly correlated with overall signal intensity and the number of identified proteins from streptavidin-enrichments. Discordant expression levels between the bait and control samples result in high-frequency false-negative and false-positive identifications. Data normalization strategies help correct these expression differences but also introduce data distortion for proteins with high or low endogenous expression. Using the ubiquitin ligases RNF10 and HUWE1 as bait proteins, we demonstrate that matching TurboID expression between control and bait proteins allows for similar sampling of non-specific interactions. Using a matched expression strategy results in significantly reduced background interference and increases the accuracy of interactome assignments. These results document the need to alter proximity-labeling experimental workflows to include the generation of matched expression controls to enhance proximity labeling proteomics interactome mapping robustness and reproducibility.
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