Cell-specific bioorthogonal tagging of glycoproteins

Author:

Cioce AnnaORCID,Calle BeatrizORCID,Rizou Tatiana,Lowery Sarah C.,Bridgeman Victoria L.,Mahoney Keira E.ORCID,Marchesi Andrea,Bineva-Todd Ganka,Flynn HelenORCID,Li Zhen,Tastan Omur Y.,Roustan Chloe,Soro-Barrio PabloORCID,Rafiee Mahmoud-Reza,Garza-Garcia AcelyORCID,Antonopoulos AristotelisORCID,Wood Thomas M.,Keenan TessaORCID,Both Peter,Huang Kun,Parmeggian FabioORCID,Snijders Ambrosius P.ORCID,Skehel MarkORCID,Kjær SvendORCID,Fascione Martin A.ORCID,Bertozzi Carolyn R.ORCID,Haslam Stuart M.ORCID,Flitsch Sabine L.ORCID,Malaker Stacy A.ORCID,Malanchi IlariaORCID,Schumann BenjaminORCID

Abstract

AbstractAltered glycoprotein expression is an undisputed corollary of cancer development. Understanding these alterations is paramount but hampered by limitations underlying cellular model systems. For instance, the intricate interactions between tumour and host cannot be adequately recapitulated in monoculture of tumour-derived cell lines. More complex co-culture models usually rely on sorting procedures for proteome analyses and rarely capture the details of protein glycosylation. Here, we report a strategy termed Bio-Orthogonal Cell line-specific Tagging of Glycoproteins (BOCTAG). Cells are equipped by transfection with an artificial biosynthetic pathway that transforms bioorthogonally tagged sugars into the corresponding nucleotide-sugars. Only transfected cells incorporate bioorthogonal tags into glycoproteins in the presence of non-transfected cells. We employ BOCTAG as an imaging technique and to annotate cell-specific glycosylation sites in mass spectrometry-glycoproteomics. We demonstrate application in co-culture and mouse models, allowing for profiling of the glycoproteome as an important modulator of cellular function.

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry,Multidisciplinary

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