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Single-pot glycoprotein biosynthesis using a cell-free transcription-translation system enriched with glycosylation machinery

The emerging discipline of bacterial glycoengineering has made it possible to produce designer glycans and glycoconjugates for use as vaccines and therapeutics. Unfortunately, cell-based production of homogeneous glycoproteins remains a significant challenge due to cell viability constraints and the...

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Autores principales: Jaroentomeechai, Thapakorn, Stark, Jessica C., Natarajan, Aravind, Glasscock, Cameron J., Yates, Laura E., Hsu, Karen J., Mrksich, Milan, Jewett, Michael C., DeLisa, Matthew P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6043479/
https://www.ncbi.nlm.nih.gov/pubmed/30002445
http://dx.doi.org/10.1038/s41467-018-05110-x
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author Jaroentomeechai, Thapakorn
Stark, Jessica C.
Natarajan, Aravind
Glasscock, Cameron J.
Yates, Laura E.
Hsu, Karen J.
Mrksich, Milan
Jewett, Michael C.
DeLisa, Matthew P.
author_facet Jaroentomeechai, Thapakorn
Stark, Jessica C.
Natarajan, Aravind
Glasscock, Cameron J.
Yates, Laura E.
Hsu, Karen J.
Mrksich, Milan
Jewett, Michael C.
DeLisa, Matthew P.
author_sort Jaroentomeechai, Thapakorn
collection PubMed
description The emerging discipline of bacterial glycoengineering has made it possible to produce designer glycans and glycoconjugates for use as vaccines and therapeutics. Unfortunately, cell-based production of homogeneous glycoproteins remains a significant challenge due to cell viability constraints and the inability to control glycosylation components at precise ratios in vivo. To address these challenges, we describe a novel cell-free glycoprotein synthesis (CFGpS) technology that seamlessly integrates protein biosynthesis with asparagine-linked protein glycosylation. This technology leverages a glyco-optimized Escherichia coli strain to source cell extracts that are selectively enriched with glycosylation components, including oligosaccharyltransferases (OSTs) and lipid-linked oligosaccharides (LLOs). The resulting extracts enable a one-pot reaction scheme for efficient and site-specific glycosylation of target proteins. The CFGpS platform is highly modular, allowing the use of multiple distinct OSTs and structurally diverse LLOs. As such, we anticipate CFGpS will facilitate fundamental understanding in glycoscience and make possible applications in on demand biomanufacturing of glycoproteins.
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spelling pubmed-60434792018-07-16 Single-pot glycoprotein biosynthesis using a cell-free transcription-translation system enriched with glycosylation machinery Jaroentomeechai, Thapakorn Stark, Jessica C. Natarajan, Aravind Glasscock, Cameron J. Yates, Laura E. Hsu, Karen J. Mrksich, Milan Jewett, Michael C. DeLisa, Matthew P. Nat Commun Article The emerging discipline of bacterial glycoengineering has made it possible to produce designer glycans and glycoconjugates for use as vaccines and therapeutics. Unfortunately, cell-based production of homogeneous glycoproteins remains a significant challenge due to cell viability constraints and the inability to control glycosylation components at precise ratios in vivo. To address these challenges, we describe a novel cell-free glycoprotein synthesis (CFGpS) technology that seamlessly integrates protein biosynthesis with asparagine-linked protein glycosylation. This technology leverages a glyco-optimized Escherichia coli strain to source cell extracts that are selectively enriched with glycosylation components, including oligosaccharyltransferases (OSTs) and lipid-linked oligosaccharides (LLOs). The resulting extracts enable a one-pot reaction scheme for efficient and site-specific glycosylation of target proteins. The CFGpS platform is highly modular, allowing the use of multiple distinct OSTs and structurally diverse LLOs. As such, we anticipate CFGpS will facilitate fundamental understanding in glycoscience and make possible applications in on demand biomanufacturing of glycoproteins. Nature Publishing Group UK 2018-07-12 /pmc/articles/PMC6043479/ /pubmed/30002445 http://dx.doi.org/10.1038/s41467-018-05110-x Text en © The Author(s) 2018 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/.
spellingShingle Article
Jaroentomeechai, Thapakorn
Stark, Jessica C.
Natarajan, Aravind
Glasscock, Cameron J.
Yates, Laura E.
Hsu, Karen J.
Mrksich, Milan
Jewett, Michael C.
DeLisa, Matthew P.
Single-pot glycoprotein biosynthesis using a cell-free transcription-translation system enriched with glycosylation machinery
title Single-pot glycoprotein biosynthesis using a cell-free transcription-translation system enriched with glycosylation machinery
title_full Single-pot glycoprotein biosynthesis using a cell-free transcription-translation system enriched with glycosylation machinery
title_fullStr Single-pot glycoprotein biosynthesis using a cell-free transcription-translation system enriched with glycosylation machinery
title_full_unstemmed Single-pot glycoprotein biosynthesis using a cell-free transcription-translation system enriched with glycosylation machinery
title_short Single-pot glycoprotein biosynthesis using a cell-free transcription-translation system enriched with glycosylation machinery
title_sort single-pot glycoprotein biosynthesis using a cell-free transcription-translation system enriched with glycosylation machinery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6043479/
https://www.ncbi.nlm.nih.gov/pubmed/30002445
http://dx.doi.org/10.1038/s41467-018-05110-x
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