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Flow Cytometric Characterization of Murine B Cell Development
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Classification of mouse B cell types using surfaceome proteotype maps.

Marc van Oostrum1,2,3,4, Maik Müller1,2,3, Fabian Klein5

  • 1Biomedical Proteomics Platform, Department of Health Sciences and Technology, ETH Zurich, 8093, Zurich, Switzerland.

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|December 18, 2019
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This summary is machine-generated.

We developed autoCSC, an automated method for mapping cell surface proteins, even with limited samples. This technology reveals new details about developing mouse B cell populations.

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Area of Science:

  • Proteomics
  • Glycomics
  • Immunology

Background:

  • Cell surface proteotype and extracellular glycosylation site identification is difficult with limited sample sizes.
  • Existing Cell Surface Capture (CSC) technology faces challenges in sensitivity, reproducibility, and throughput.

Purpose of the Study:

  • To miniaturize and automate the Cell Surface Capture (CSC) technology for enhanced performance.
  • To create population-specific surfaceome maps of developing mouse B cells.
  • To identify novel developmental cell subpopulations using targeted flow cytometry.

Main Methods:

  • Miniaturization and automation of the Cell Surface Capture (CSC) technology, termed autoCSC.
  • Application of autoCSC to generate surfaceome maps of developing mouse B cells.
  • Utilizing targeted flow cytometry for subpopulation identification.

Main Results:

  • autoCSC significantly increases sensitivity, reproducibility, and throughput compared to the original CSC method.
  • Population-specific surfaceome maps of developing mouse B cells were successfully generated.
  • Targeted flow cytometry identified previously unknown developmental cell subpopulations.

Conclusions:

  • The automated CSC (autoCSC) technology provides a more sensitive and efficient approach for cell surface proteotype analysis.
  • autoCSC enables detailed mapping of cell surfaces, aiding in the discovery of cellular heterogeneity.
  • This technology advances the study of cell development and subpopulation identification in systems biology.