Cargando…
Modeling Glycan Processing Reveals Golgi-Enzyme Homeostasis upon Trafficking Defects and Cellular Differentiation
The decoration of proteins by carbohydrates is essential for eukaryotic life yet heterogeneous due to a lack of biosynthetic templates. This complex carbohydrate mixture—the glycan profile—is generated in the compartmentalized Golgi, in which level and localization of glycosylation enzymes are key d...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6486481/ https://www.ncbi.nlm.nih.gov/pubmed/31018136 http://dx.doi.org/10.1016/j.celrep.2019.03.107 |
_version_ | 1783414346275094528 |
---|---|
author | Fisher, Peter Spencer, Hannah Thomas-Oates, Jane Wood, A. Jamie Ungar, Daniel |
author_facet | Fisher, Peter Spencer, Hannah Thomas-Oates, Jane Wood, A. Jamie Ungar, Daniel |
author_sort | Fisher, Peter |
collection | PubMed |
description | The decoration of proteins by carbohydrates is essential for eukaryotic life yet heterogeneous due to a lack of biosynthetic templates. This complex carbohydrate mixture—the glycan profile—is generated in the compartmentalized Golgi, in which level and localization of glycosylation enzymes are key determinants. Here, we develop and validate a computational model for glycan biosynthesis to probe how the biosynthetic machinery creates different glycan profiles. We combined stochastic modeling with Bayesian fitting that enables rigorous comparison to experimental data despite starting with uncertain initial parameters. This is an important development in the field of glycan modeling, which revealed biological insights about the glycosylation machinery in altered cellular states. We experimentally validated changes in N-linked glycan-modifying enzymes in cells with perturbed intra-Golgi-enzyme sorting and the predicted glycan-branching activity during osteogenesis. Our model can provide detailed information on altered biosynthetic paths, with potential for advancing treatments for glycosylation-related diseases and glyco-engineering of cells. |
format | Online Article Text |
id | pubmed-6486481 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-64864812019-05-02 Modeling Glycan Processing Reveals Golgi-Enzyme Homeostasis upon Trafficking Defects and Cellular Differentiation Fisher, Peter Spencer, Hannah Thomas-Oates, Jane Wood, A. Jamie Ungar, Daniel Cell Rep Article The decoration of proteins by carbohydrates is essential for eukaryotic life yet heterogeneous due to a lack of biosynthetic templates. This complex carbohydrate mixture—the glycan profile—is generated in the compartmentalized Golgi, in which level and localization of glycosylation enzymes are key determinants. Here, we develop and validate a computational model for glycan biosynthesis to probe how the biosynthetic machinery creates different glycan profiles. We combined stochastic modeling with Bayesian fitting that enables rigorous comparison to experimental data despite starting with uncertain initial parameters. This is an important development in the field of glycan modeling, which revealed biological insights about the glycosylation machinery in altered cellular states. We experimentally validated changes in N-linked glycan-modifying enzymes in cells with perturbed intra-Golgi-enzyme sorting and the predicted glycan-branching activity during osteogenesis. Our model can provide detailed information on altered biosynthetic paths, with potential for advancing treatments for glycosylation-related diseases and glyco-engineering of cells. Cell Press 2019-04-23 /pmc/articles/PMC6486481/ /pubmed/31018136 http://dx.doi.org/10.1016/j.celrep.2019.03.107 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Fisher, Peter Spencer, Hannah Thomas-Oates, Jane Wood, A. Jamie Ungar, Daniel Modeling Glycan Processing Reveals Golgi-Enzyme Homeostasis upon Trafficking Defects and Cellular Differentiation |
title | Modeling Glycan Processing Reveals Golgi-Enzyme Homeostasis upon Trafficking Defects and Cellular Differentiation |
title_full | Modeling Glycan Processing Reveals Golgi-Enzyme Homeostasis upon Trafficking Defects and Cellular Differentiation |
title_fullStr | Modeling Glycan Processing Reveals Golgi-Enzyme Homeostasis upon Trafficking Defects and Cellular Differentiation |
title_full_unstemmed | Modeling Glycan Processing Reveals Golgi-Enzyme Homeostasis upon Trafficking Defects and Cellular Differentiation |
title_short | Modeling Glycan Processing Reveals Golgi-Enzyme Homeostasis upon Trafficking Defects and Cellular Differentiation |
title_sort | modeling glycan processing reveals golgi-enzyme homeostasis upon trafficking defects and cellular differentiation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6486481/ https://www.ncbi.nlm.nih.gov/pubmed/31018136 http://dx.doi.org/10.1016/j.celrep.2019.03.107 |
work_keys_str_mv | AT fisherpeter modelingglycanprocessingrevealsgolgienzymehomeostasisupontraffickingdefectsandcellulardifferentiation AT spencerhannah modelingglycanprocessingrevealsgolgienzymehomeostasisupontraffickingdefectsandcellulardifferentiation AT thomasoatesjane modelingglycanprocessingrevealsgolgienzymehomeostasisupontraffickingdefectsandcellulardifferentiation AT woodajamie modelingglycanprocessingrevealsgolgienzymehomeostasisupontraffickingdefectsandcellulardifferentiation AT ungardaniel modelingglycanprocessingrevealsgolgienzymehomeostasisupontraffickingdefectsandcellulardifferentiation |