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  MS-Based Proteomics of Body Fluids: The End of the Beginning

Bader, J. M., Albrecht, V., & Mann, M. (2023). MS-Based Proteomics of Body Fluids: The End of the Beginning. Molecular & Cellular Proteomics, 22(7):. doi:10.1016/j.mcpro.2023.100577.

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基本情報

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アイテムのパーマリンク: https://hdl.handle.net/21.11116/0000-000E-7F91-0 版のパーマリンク: https://hdl.handle.net/21.11116/0000-0010-6F83-E
資料種別: 学術論文

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 作成者:
Bader, Jakob Maximilian1, 著者           
Albrecht, Vincent1, 著者           
Mann, M.1, 著者           
所属:
1Mann, Matthias / Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Max Planck Society, ou_1565159              

内容説明

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キーワード: tandem mass-spectrometry biomarker discovery plasma proteome proteins quantification serum fragmentation validation throughput framework Biochemistry & Molecular Biology
 要旨: Accurate biomarkers are a crucial and necessary precondition for precision medicine, yet existing ones are often unspecific and new ones have been very slow to enter the clinic. Mass spectrometry (MS) -based proteomics excels by its untargeted nature, specificity of identification, and quantification, making it an ideal technology for biomarker discovery and routine measurement. It has unique attributes compared to affinity binder technologies, such as OLINK Proximity Extension Assay and SOMAscan. In in a previous review in 2017, we described technological and conceptual limitations that had held back success. We proposed a 'rectangular strategy' to better separate true biomarkers by minimizing cohortspecific effects. Today, this has converged with advances in MS -based proteomics technology, such as increased sample throughput, depth of identification, and quantification. As a result, biomarker discovery studies have become more successful, producing biomarker candidates that withstand independent verification and, in some cases, already outperform state-of-the-art clinical assays. We summarize developments over the last years, including the benefits of large and independent cohorts, which are necessary for clinical acceptance. Shorter gradients, new scan modes, and multiplexing are about to drastically increase throughput, cross -study integration, and quantification, including proxies for absolute levels. We have found that multiprotein panels are inherently more robust than current single analyte tests and better capture the complexity of human phenotypes. Routine MS measurement in the clinic is fast becoming a viable option. The full set of proteins in a body fluid (global proteome) is the most important reference and the best process control. Additionally, it increasingly has all the information that could be obtained from targeted analysis although the latter may be the most straightforward way to enter regular use. Many challenges remain, not least of a regulatory and ethical nature, but the outlook for MS -based clinical applications has never been brighter.

資料詳細

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言語: eng - English
 日付: 2023-07-01
 出版の状態: 出版
 ページ: -
 出版情報: -
 目次: -
 査読: -
 識別子(DOI, ISBNなど): その他: WOS:001162962600001
DOI: 10.1016/j.mcpro.2023.100577
 学位: -

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出版物 1

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出版物名: Molecular & Cellular Proteomics
  その他 : Mol Cell Proteomics
  その他 : Molecular and Cellular Proteomics
  省略形 : MCP
種別: 学術雑誌
 著者・編者:
所属:
出版社, 出版地: Bethesda, MD : Elsevier ; American Society for Biochemistry and Molecular Biology (ASBMB)
ページ: - 巻号: 22 (7) 通巻号: 100577 開始・終了ページ: - 識別子(ISBN, ISSN, DOIなど): ISSN: 1535-9476
CoNE: https://pure.mpg.de/cone/journals/resource/111035577487002