IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v12y2021i1d10.1038_s41467-021-23667-y.html
   My bibliography  Save this article

Quantitative single-cell proteomics as a tool to characterize cellular hierarchies

Author

Listed:
  • Erwin M. Schoof

    (University of Copenhagen
    Biotech Research and Innovation Centre (BRIC), University of Copenhagen
    Technical University of Denmark
    University of Copenhagen)

  • Benjamin Furtwängler

    (University of Copenhagen
    Biotech Research and Innovation Centre (BRIC), University of Copenhagen
    University of Copenhagen)

  • Nil Üresin

    (University of Copenhagen
    Biotech Research and Innovation Centre (BRIC), University of Copenhagen
    University of Copenhagen)

  • Nicolas Rapin

    (University of Copenhagen
    Biotech Research and Innovation Centre (BRIC), University of Copenhagen
    University of Copenhagen)

  • Simonas Savickas

    (Technical University of Denmark)

  • Coline Gentil

    (University of Copenhagen
    Biotech Research and Innovation Centre (BRIC), University of Copenhagen)

  • Eric Lechman

    (Princess Margaret Cancer Centre, University Health Network
    University of Toronto)

  • Ulrich auf dem Keller

    (Technical University of Denmark)

  • John E. Dick

    (Princess Margaret Cancer Centre, University Health Network
    University of Toronto)

  • Bo T. Porse

    (University of Copenhagen
    Biotech Research and Innovation Centre (BRIC), University of Copenhagen
    University of Copenhagen)

Abstract

Large-scale single-cell analyses are of fundamental importance in order to capture biological heterogeneity within complex cell systems, but have largely been limited to RNA-based technologies. Here we present a comprehensive benchmarked experimental and computational workflow, which establishes global single-cell mass spectrometry-based proteomics as a tool for large-scale single-cell analyses. By exploiting a primary leukemia model system, we demonstrate both through pre-enrichment of cell populations and through a non-enriched unbiased approach that our workflow enables the exploration of cellular heterogeneity within this aberrant developmental hierarchy. Our approach is capable of consistently quantifying ~1000 proteins per cell across thousands of individual cells using limited instrument time. Furthermore, we develop a computational workflow (SCeptre) that effectively normalizes the data, integrates available FACS data and facilitates downstream analysis. The approach presented here lays a foundation for implementing global single-cell proteomics studies across the world.

Suggested Citation

  • Erwin M. Schoof & Benjamin Furtwängler & Nil Üresin & Nicolas Rapin & Simonas Savickas & Coline Gentil & Eric Lechman & Ulrich auf dem Keller & John E. Dick & Bo T. Porse, 2021. "Quantitative single-cell proteomics as a tool to characterize cellular hierarchies," Nature Communications, Nature, vol. 12(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-23667-y
    DOI: 10.1038/s41467-021-23667-y
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-021-23667-y
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-021-23667-y?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    Citations

    Citations are extracted by the CitEc Project, subscribe to its RSS feed for this item.
    as


    Cited by:

    1. Kim Theilgaard-Mönch & Sachin Pundhir & Kristian Reckzeh & Jinyu Su & Marta Tapia & Benjamin Furtwängler & Johan Jendholm & Janus Schou Jakobsen & Marie Sigurd Hasemann & Kasper Jermiin Knudsen & Jack, 2022. "Transcription factor-driven coordination of cell cycle exit and lineage-specification in vivo during granulocytic differentiation," Nature Communications, Nature, vol. 13(1), pages 1-17, December.
    2. Anna Cioce & Beatriz Calle & Tatiana Rizou & Sarah C. Lowery & Victoria L. Bridgeman & Keira E. Mahoney & Andrea Marchesi & Ganka Bineva-Todd & Helen Flynn & Zhen Li & Omur Y. Tastan & Chloe Roustan &, 2022. "Cell-specific bioorthogonal tagging of glycoproteins," Nature Communications, Nature, vol. 13(1), pages 1-18, December.
    3. Christina Bligaard Pedersen & Søren Helweg Dam & Mike Bogetofte Barnkob & Michael D. Leipold & Noelia Purroy & Laura Z. Rassenti & Thomas J. Kipps & Jennifer Nguyen & James Arthur Lederer & Satyen Har, 2022. "cyCombine allows for robust integration of single-cell cytometry datasets within and across technologies," Nature Communications, Nature, vol. 13(1), pages 1-12, December.
    4. Benjamin C. Orsburn & Yuting Yuan & Namandjé N. Bumpus, 2022. "Insights into protein post-translational modification landscapes of individual human cells by trapped ion mobility time-of-flight mass spectrometry," Nature Communications, Nature, vol. 13(1), pages 1-14, December.
    5. Yu Wang & Zhi-Ying Guan & Shao-Wen Shi & Yi-Rong Jiang & Jie Zhang & Yi Yang & Qiong Wu & Jie Wu & Jian-Bo Chen & Wei-Xin Ying & Qin-Qin Xu & Qian-Xi Fan & Hui-Feng Wang & Li Zhou & Ling Wang & Jin Fa, 2024. "Pick-up single-cell proteomic analysis for quantifying up to 3000 proteins in a Mammalian cell," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
    6. Jongmin Woo & Sarah M. Williams & Lye Meng Markillie & Song Feng & Chia-Feng Tsai & Victor Aguilera-Vazquez & Ryan L. Sontag & Ronald J. Moore & Dehong Hu & Hardeep S. Mehta & Joshua Cantlon-Bruce & T, 2021. "High-throughput and high-efficiency sample preparation for single-cell proteomics using a nested nanowell chip," Nature Communications, Nature, vol. 12(1), pages 1-11, December.
    7. Valdemaras Petrosius & Pedro Aragon-Fernandez & Nil Üresin & Gergo Kovacs & Teeradon Phlairaharn & Benjamin Furtwängler & Jeff Op De Beeck & Sarah L. Skovbakke & Steffen Goletz & Simon Francis Thomsen, 2023. "Exploration of cell state heterogeneity using single-cell proteomics through sensitivity-tailored data-independent acquisition," Nature Communications, Nature, vol. 14(1), pages 1-16, December.
    8. Manuel Matzinger & Anna Schmücker & Ramesh Yelagandula & Karel Stejskal & Gabriela Krššáková & Frédéric Berger & Karl Mechtler & Rupert L. Mayer, 2024. "Micropillar arrays, wide window acquisition and AI-based data analysis improve comprehensiveness in multiple proteomic applications," Nature Communications, Nature, vol. 15(1), pages 1-17, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-23667-y. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.