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Cell-specific bioorthogonal tagging of glycoproteins.
Cioce, Anna; Calle, Beatriz; Rizou, Tatiana; Lowery, Sarah C; Bridgeman, Victoria L; Mahoney, Keira E; Marchesi, Andrea; Bineva-Todd, Ganka; Flynn, Helen; Li, Zhen; Tastan, Omur Y; Roustan, Chloe; Soro-Barrio, Pablo; Rafiee, Mahmoud-Reza; Garza-Garcia, Acely; Antonopoulos, Aristotelis; Wood, Thomas M; Keenan, Tessa; Both, Peter; Huang, Kun; Parmeggian, Fabio; Snijders, Ambrosius P; Skehel, Mark; Kjær, Svend; Fascione, Martin A; Bertozzi, Carolyn R; Haslam, Stuart M; Flitsch, Sabine L; Malaker, Stacy A; Malanchi, Ilaria; Schumann, Benjamin.
Afiliación
  • Cioce A; Department of Chemistry, Imperial College London, London, W12 0BZ, UK.
  • Calle B; Chemical Glycobiology Laboratory, The Francis Crick Institute, London, NW1 1AT, UK.
  • Rizou T; Department of Chemistry, Imperial College London, London, W12 0BZ, UK.
  • Lowery SC; Chemical Glycobiology Laboratory, The Francis Crick Institute, London, NW1 1AT, UK.
  • Bridgeman VL; Tumour-Host Interaction Laboratory, The Francis Crick Institute, London, NW1 1AT, UK.
  • Mahoney KE; Tumour-Host Interaction Laboratory, The Francis Crick Institute, London, NW1 1AT, UK.
  • Marchesi A; Department of Chemistry, Yale University, New Haven, CT 06511, USA.
  • Bineva-Todd G; Tumour-Host Interaction Laboratory, The Francis Crick Institute, London, NW1 1AT, UK.
  • Flynn H; Department of Chemistry, Yale University, New Haven, CT 06511, USA.
  • Li Z; Department of Chemistry, Imperial College London, London, W12 0BZ, UK.
  • Tastan OY; Chemical Glycobiology Laboratory, The Francis Crick Institute, London, NW1 1AT, UK.
  • Roustan C; Chemical Glycobiology Laboratory, The Francis Crick Institute, London, NW1 1AT, UK.
  • Soro-Barrio P; Proteomics Science Technology Platform, The Francis Crick Institute, London, NW1 1AT, UK.
  • Rafiee MR; Department of Chemistry, Imperial College London, London, W12 0BZ, UK.
  • Garza-Garcia A; Chemical Glycobiology Laboratory, The Francis Crick Institute, London, NW1 1AT, UK.
  • Antonopoulos A; Chemical Glycobiology Laboratory, The Francis Crick Institute, London, NW1 1AT, UK.
  • Wood TM; Structural Biology Science Technology Platform, The Francis Crick Institute, London, NW1 1AT, UK.
  • Keenan T; Bioinformatics & Biostatistics Science Technology Platform, The Francis Crick Institute, London, NW1 1AT, UK.
  • Both P; RNA Networks Laboratory, The Francis Crick Institute, London, NW1 1AT, UK.
  • Huang K; Mycobacterial Metabolism and Antibiotic Research Laboratory, The Francis Crick Institute, London, NW1 1AT, UK.
  • Parmeggian F; Department of Life Sciences, Imperial College London, London, SW7 2AZ, UK.
  • Snijders AP; Sarafan ChEM-H, Department of Chemistry and Howard Hughes Medical Institute, Stanford University, Stanford, CA 94305, USA.
  • Skehel M; Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
  • Kjær S; Department of Chemistry, University of York, York, YO10 5DD, UK.
  • Fascione MA; School of Chemistry & Institute of Biotechnology, The University of Manchester, Manchester, M1 7DN, UK.
  • Bertozzi CR; R&D Department, Axxence Slovakia s.r.o., 81107, Bratislava, Slovakia.
  • Haslam SM; School of Chemistry & Institute of Biotechnology, The University of Manchester, Manchester, M1 7DN, UK.
  • Flitsch SL; Department of Chemistry and Biochemistry, University of Maryland, College Park, MD 20742, USA.
  • Malaker SA; School of Chemistry & Institute of Biotechnology, The University of Manchester, Manchester, M1 7DN, UK.
  • Malanchi I; Department of Chemistry, Materials and Chemical Engineering "G. Natta", Politecnico di Milano, 20131, Milano, Italy.
  • Schumann B; Proteomics Science Technology Platform, The Francis Crick Institute, London, NW1 1AT, UK.
Nat Commun ; 13(1): 6237, 2022 10 25.
Article en En | MEDLINE | ID: mdl-36284108
ABSTRACT
Altered 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.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteoma / Proteómica Límite: Animals Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteoma / Proteómica Límite: Animals Idioma: En Año: 2022 Tipo del documento: Article