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GproDIA enables data-independent acquisition glycoproteomics with comprehensive statistical control

Author

Listed:
  • Yi Yang

    (Fudan University)

  • Guoquan Yan

    (Fudan University)

  • Siyuan Kong

    (Fudan University)

  • Mengxi Wu

    (Fudan University)

  • Pengyuan Yang

    (Fudan University
    Fudan University
    Fudan University
    Fudan University)

  • Weiqian Cao

    (Fudan University
    Fudan University
    Fudan University
    Fudan University)

  • Liang Qiao

    (Fudan University)

Abstract

Large-scale profiling of intact glycopeptides is critical but challenging in glycoproteomics. Data independent acquisition (DIA) is an emerging technology with deep proteome coverage and accurate quantitative capability in proteomics studies, but is still in the early stage of development in the field of glycoproteomics. We propose GproDIA, a framework for the proteome-wide characterization of intact glycopeptides from DIA data with comprehensive statistical control by a 2-dimentional false discovery rate approach and a glycoform inference algorithm, enabling accurate identification of intact glycopeptides using wide isolation windows. We further utilize a semi-empirical spectrum prediction strategy to expand the coverage of spectral libraries of glycopeptides. We benchmark our method for N-glycopeptide profiling on DIA data of yeast and human serum samples, demonstrating that DIA with GproDIA outperforms the data-dependent acquisition-based methods for glycoproteomics in terms of capacity and data completeness of identification, as well as accuracy and precision of quantification. We expect that this work can provide a powerful tool for glycoproteomic studies.

Suggested Citation

  • Yi Yang & Guoquan Yan & Siyuan Kong & Mengxi Wu & Pengyuan Yang & Weiqian Cao & Liang Qiao, 2021. "GproDIA enables data-independent acquisition glycoproteomics with comprehensive statistical control," Nature Communications, Nature, vol. 12(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-26246-3
    DOI: 10.1038/s41467-021-26246-3
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    References listed on IDEAS

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    1. Lukas Wettstein & Tatjana Weil & Carina Conzelmann & Janis A. Müller & Rüdiger Groß & Maximilian Hirschenberger & Alina Seidel & Susanne Klute & Fabian Zech & Caterina Prelli Bozzo & Nico Preising & G, 2021. "Alpha-1 antitrypsin inhibits TMPRSS2 protease activity and SARS-CoV-2 infection," Nature Communications, Nature, vol. 12(1), pages 1-10, December.
    2. Yi Yang & Xiaohui Liu & Chengpin Shen & Yu Lin & Pengyuan Yang & Liang Qiao, 2020. "In silico spectral libraries by deep learning facilitate data-independent acquisition proteomics," Nature Communications, Nature, vol. 11(1), pages 1-11, December.
    3. Ben C. Collins & Christie L. Hunter & Yansheng Liu & Birgit Schilling & George Rosenberger & Samuel L. Bader & Daniel W. Chan & Bradford W. Gibson & Anne-Claude Gingras & Jason M. Held & Mio Hirayama-, 2017. "Multi-laboratory assessment of reproducibility, qualitative and quantitative performance of SWATH-mass spectrometry," Nature Communications, Nature, vol. 8(1), pages 1-12, December.
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    Cited by:

    1. Yi Yang & Qun Fang, 2024. "Prediction of glycopeptide fragment mass spectra by deep learning," Nature Communications, Nature, vol. 15(1), pages 1-12, December.
    2. Siyuan Kong & Pengyun Gong & Wen-Feng Zeng & Biyun Jiang & Xinhang Hou & Yang Zhang & Huanhuan Zhao & Mingqi Liu & Guoquan Yan & Xinwen Zhou & Xihua Qiao & Mengxi Wu & Pengyuan Yang & Chao Liu & Weiqi, 2022. "pGlycoQuant with a deep residual network for quantitative glycoproteomics at intact glycopeptide level," Nature Communications, Nature, vol. 13(1), pages 1-17, December.
    3. Klemens Fröhlich & Eva Brombacher & Matthias Fahrner & Daniel Vogele & Lucas Kook & Niko Pinter & Peter Bronsert & Sylvia Timme-Bronsert & Alexander Schmidt & Katja Bärenfaller & Clemens Kreutz & Oliv, 2022. "Benchmarking of analysis strategies for data-independent acquisition proteomics using a large-scale dataset comprising inter-patient heterogeneity," Nature Communications, Nature, vol. 13(1), pages 1-13, December.

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