使用表达式匹配控制实现高置信度基于接近的交互组分类。

IF 5.5 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Molecular & Cellular Proteomics Pub Date : 2025-07-01 Epub Date: 2025-05-27 DOI:10.1016/j.mcpro.2025.101001
Fulin Jiang, Xuezhen Ge, Eric J Bennett
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引用次数: 0

摘要

近距离标记方法已被广泛用于定义蛋白质相互作用组。由于使用基于turboid的方法进行接近标记的固有混杂性,识别和采用适当的标记控制是减轻背景干扰和提高相互作用组分配准确性的关键步骤。在这里,我们评估了表达式控制和数据规范化策略在生成高置信度交互组图方面的有效性。我们证明,控制TurboID蛋白表达的程度与总体信号强度和链霉亲和素富集鉴定的蛋白数量密切相关。诱饵和对照样本之间的表达水平不一致导致高频率的假阴性和假阳性鉴定。数据规范化策略有助于纠正这些表达差异,但也会引入具有高或低内源性表达的蛋白质的数据失真。使用泛素连接酶RNF10和HUWE1作为诱饵蛋白,我们证明在对照蛋白和诱饵蛋白之间匹配TurboID表达允许类似的非特异性相互作用取样。使用匹配表达策略可以显著减少背景干扰,提高互作组分配的准确性。这些结果证明需要改变接近标记实验工作流程,包括生成匹配的表达控制,以增强接近标记蛋白质组学相互作用组映射的稳健性和可重复性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Employing Expression-Matched Controls Enables High-Confidence Proximity-Based Interactome Classification.

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.

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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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