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  Trapped Ion Mobility Spectrometry and Parallel Accumulation-Serial Fragmentation in Proteomics

Meier, F., Park, M. A., & Mann, M. (2021). Trapped Ion Mobility Spectrometry and Parallel Accumulation-Serial Fragmentation in Proteomics. Molecular and Cellular Proteomics, 20:. doi:10.1016/j.mcpro.2021.100138.

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アイテムのパーマリンク: https://hdl.handle.net/21.11116/0000-0009-5DEA-8 版のパーマリンク: https://hdl.handle.net/21.11116/0000-0009-5DEB-7
資料種別: 学術論文

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 作成者:
Meier, Florian1, 著者           
Park, Melvin A.2, 著者
Mann, Matthias1, 著者           
所属:
1Mann, Matthias / Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Max Planck Society, ou_1565159              
2external, ou_persistent22              

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キーワード: DATA-INDEPENDENT ACQUISITION; MASS-SPECTROMETRY; HIGH-RESOLUTION; PEPTIDE IDENTIFICATION; DYNAMIC-RANGE; MS; FUNDAMENTALS; SENSITIVITY; PERFORMANCE; SEPARATIONBiochemistry & Molecular Biology;
 要旨: Recent advances in efficiency and ease of implementation have rekindled interest in ion mobility spectrometry, a technique that separates gas phase ions by their size and shape and that can be hybridized with conventional LC and MS. Here, we review the recent development of trapped ion mobility spectrometry (TIMS) coupled to TOF mass analysis. In particular, the parallel accumulation-serial fragmentation (PASEF) operation mode offers unique advantages in terms of sequencing speed and sensitivity. Its defining feature is that it synchronizes the release of ions from the TIMS device with the downstream selection of precursors for fragmentation in a TIMS quadrupole TOF configuration. As ions are compressed into narrow ion mobility peaks, the number of peptide fragment ion spectra obtained in data-dependent or targeted analyses can be increased by an order of magnitude without compromising sensitivity. Taking advantage of the correlation between ion mobility and mass, the PASEF principle also multiplies the efficiency of data-independent acquisition. This makes the technology well suited for rapid proteome profiling, an increasingly important attribute in clinical proteomics, as well as for ultrasensitive measurements down to single cells. The speed and accuracy of TIMS and PASEF also enable precise measurements of collisional cross section values at the scale of more than a million data points and the development of neural networks capable of predicting them based only on peptide sequences. Peptide collisional cross section values can differ for isobaric sequences or positional isomers of post-translational modifications. This additional information may be leveraged in real time to direct data acquisition or in postprocessing to increase confidence in peptide identifications. These developments make TIMS quadrupole TOF PASEF a powerful and expandable platform for proteomics and beyond.

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言語: eng - English
 日付: 2021
 出版の状態: オンラインで出版済み
 ページ: 13
 出版情報: -
 目次: -
 査読: 査読あり
 識別子(DOI, ISBNなど): ISI: 000697557300001
DOI: 10.1016/j.mcpro.2021.100138
 学位: -

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出版物 1

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出版物名: Molecular and Cellular Proteomics
種別: 学術雑誌
 著者・編者:
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出版社, 出版地: Bethesda, MD : American Society for Biochemistry and Molecular Biology
ページ: - 巻号: 20 通巻号: 100138 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