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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
---|---|
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 |