Article abstract


Nature Biotechnology 27, 378 - 386 (2009)
Published online: 6 April 2009 | Corrected online: 9 September 2009 | doi:10.1038/nbt.1532



There is a Corrigenda (September 2009) associated with this Article.

Mass-spectrometric identification and relative quantification of N-linked cell surface glycoproteins

Bernd Wollscheid1,4, Damaris Bausch-Fluck1,4, Christine Henderson1, Robert O'Brien1, Miriam Bibel2, Ralph Schiess3, Ruedi Aebersold1,3 & Julian D Watts1


Although the classification of cell types often relies on the identification of cell surface proteins as differentiation markers, flow cytometry requires suitable antibodies and currently permits detection of only up to a dozen differentiation markers in a single measurement. We use multiplexed mass-spectrometric identification of several hundred N-linked glycosylation sites specifically from cell surface–exposed glycoproteins to phenotype cells without antibodies in an unbiased fashion and without a priori knowledge. We apply our cell surface–capturing (CSC) technology, which covalently labels extracellular glycan moieties on live cells, to the detection and relative quantitative comparison of the cell surface N-glycoproteomes of T and B cells, as well as to monitor changes in the abundance of cell surface N-glycoprotein markers during T-cell activation and the controlled differentiation of embryonic stem cells into the neural lineage. A snapshot view of the cell surface N-glycoproteins will enable detection of panels of N-glycoproteins as potential differentiation markers that are currently not accessible by other means.

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  1. Institute for Systems Biology, Seattle, Washington, USA.
  2. Neurodegeneration Department, Neuroscience Research, Novartis Institutes for BioMedical Research, Basel, Switzerland.
  3. Institute of Molecular Systems Biology, ETHZ, Faculty of Natural Sciences, University of Zurich, Switzerland and Center for Systems Physiology and Metabolic Disease, Zurich, Switzerland.
  4. Institute of Molecular Systems Biology, ETHZ and NCCR Neuro Center for Proteomics, University of Zurich, Switzerland.

Correspondence to: Bernd Wollscheid1,4 e-mail: bernd.wollscheid@imsb.biol.ethz.ch

* In the version of this article initially published, in Methods, p.385, line 5, the concentration of MgCl2, given as 0.5 M, is incorrect. The correct concentration is 0.5 mM MgCl2.The error has been corrected in the HTML and PDF versions of the article.

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