Cargando…

Cell-specific bioorthogonal tagging of glycoproteins

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 monocul...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9596482/
https://www.ncbi.nlm.nih.gov/pubmed/36284108
http://dx.doi.org/10.1038/s41467-022-33854-0
_version_ 1784815881162850304
author 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
author_facet 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
author_sort Cioce, Anna
collection PubMed
description 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.
format Online
Article
Text
id pubmed-9596482
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-95964822022-10-27 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 Nat Commun Article 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. Nature Publishing Group UK 2022-10-25 /pmc/articles/PMC9596482/ /pubmed/36284108 http://dx.doi.org/10.1038/s41467-022-33854-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
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
Cell-specific bioorthogonal tagging of glycoproteins
title Cell-specific bioorthogonal tagging of glycoproteins
title_full Cell-specific bioorthogonal tagging of glycoproteins
title_fullStr Cell-specific bioorthogonal tagging of glycoproteins
title_full_unstemmed Cell-specific bioorthogonal tagging of glycoproteins
title_short Cell-specific bioorthogonal tagging of glycoproteins
title_sort cell-specific bioorthogonal tagging of glycoproteins
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9596482/
https://www.ncbi.nlm.nih.gov/pubmed/36284108
http://dx.doi.org/10.1038/s41467-022-33854-0
work_keys_str_mv AT cioceanna cellspecificbioorthogonaltaggingofglycoproteins
AT callebeatriz cellspecificbioorthogonaltaggingofglycoproteins
AT rizoutatiana cellspecificbioorthogonaltaggingofglycoproteins
AT lowerysarahc cellspecificbioorthogonaltaggingofglycoproteins
AT bridgemanvictorial cellspecificbioorthogonaltaggingofglycoproteins
AT mahoneykeirae cellspecificbioorthogonaltaggingofglycoproteins
AT marchesiandrea cellspecificbioorthogonaltaggingofglycoproteins
AT binevatoddganka cellspecificbioorthogonaltaggingofglycoproteins
AT flynnhelen cellspecificbioorthogonaltaggingofglycoproteins
AT lizhen cellspecificbioorthogonaltaggingofglycoproteins
AT tastanomury cellspecificbioorthogonaltaggingofglycoproteins
AT roustanchloe cellspecificbioorthogonaltaggingofglycoproteins
AT sorobarriopablo cellspecificbioorthogonaltaggingofglycoproteins
AT rafieemahmoudreza cellspecificbioorthogonaltaggingofglycoproteins
AT garzagarciaacely cellspecificbioorthogonaltaggingofglycoproteins
AT antonopoulosaristotelis cellspecificbioorthogonaltaggingofglycoproteins
AT woodthomasm cellspecificbioorthogonaltaggingofglycoproteins
AT keenantessa cellspecificbioorthogonaltaggingofglycoproteins
AT bothpeter cellspecificbioorthogonaltaggingofglycoproteins
AT huangkun cellspecificbioorthogonaltaggingofglycoproteins
AT parmeggianfabio cellspecificbioorthogonaltaggingofglycoproteins
AT snijdersambrosiusp cellspecificbioorthogonaltaggingofglycoproteins
AT skehelmark cellspecificbioorthogonaltaggingofglycoproteins
AT kjærsvend cellspecificbioorthogonaltaggingofglycoproteins
AT fascionemartina cellspecificbioorthogonaltaggingofglycoproteins
AT bertozzicarolynr cellspecificbioorthogonaltaggingofglycoproteins
AT haslamstuartm cellspecificbioorthogonaltaggingofglycoproteins
AT flitschsabinel cellspecificbioorthogonaltaggingofglycoproteins
AT malakerstacya cellspecificbioorthogonaltaggingofglycoproteins
AT malanchiilaria cellspecificbioorthogonaltaggingofglycoproteins
AT schumannbenjamin cellspecificbioorthogonaltaggingofglycoproteins