提高交联质谱可靠性和数据共享的路线图。

IF 5.5 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Juri Rappsilber, James Bruce, Colin Combe, Stephen Fried, Andrea Graziadei, Albert J R Heck, Claudio Iacobucci, Alexander Leitner, Karl Mechtler, Petr Novak, Francis O'Reilly, David C Schriemer, Andrea Sinz, Florian Stengel, Konstantinos Thalassinos
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引用次数: 0

摘要

交联质谱(MS)可以揭示蛋白质之间的相互作用,并提供蛋白质在其原生细胞环境中的结构信息。尽管前景光明,但由于数据格式不一致、错误控制方法多变以及与全球数据存储库的互操作性不足,该领域仍然受到阻碍。最近的进展,特别是在错误发现率(FDR)模型和管道基准测试方面,表明交联质谱数据可以达到符合整合结构生物学需求的可靠性。然而,为了推动有意义的进展,社区必须就错误估计、开放数据格式和简化的存储库提交达成一致。这种观点强调了这些挑战,澄清了剩余的障碍,并提出了切实可行的下一步措施。成功的领域协调将提高交联质谱在更广泛的生物界中的接受度,并且对于数据的可靠性至关重要,无论数据来自何处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Roadmap for Improving Reliability and Data Sharing in Crosslinking Mass Spectrometry.

Crosslinking Mass Spectrometry (MS) can uncover protein-protein interactions and provide structural information on proteins in their native cellular environments. Despite its promise, the field remains hampered by inconsistent data formats, variable approaches to error control, and insufficient interoperability with global data repositories. Recent advances, especially in false discovery rate (FDR) models and pipeline benchmarking, show that Crosslinking MS data can reach a reliability that matches the demand of integrative structural biology. To drive meaningful progress, however, the community must agree on error estimation, open data formats, and streamlined repository submissions. This perspective highlights these challenges, clarifies remaining barriers, and frames practical next steps. Successful field harmonisation will enhance the acceptance of Crosslinking MS in the broader biological community and is critical for the dependability of the data, no matter where it is produced.

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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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