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Total Synthesis of Polysaccharides by Automated Glycan Assembly
[Image: see text] Polysaccharides are the most abundant biopolymers on earth that serve various structural and modulatory functions. Pure, completely defined linear and branched polysaccharides are essential to understand carbohydrate structure and function. Polysaccharide isolation provides heterog...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7304863/ https://www.ncbi.nlm.nih.gov/pubmed/32338884 http://dx.doi.org/10.1021/jacs.0c00751 |
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author | Joseph, A. Abragam Pardo-Vargas, Alonso Seeberger, Peter H. |
author_facet | Joseph, A. Abragam Pardo-Vargas, Alonso Seeberger, Peter H. |
author_sort | Joseph, A. Abragam |
collection | PubMed |
description | [Image: see text] Polysaccharides are the most abundant biopolymers on earth that serve various structural and modulatory functions. Pure, completely defined linear and branched polysaccharides are essential to understand carbohydrate structure and function. Polysaccharide isolation provides heterogeneous mixtures, while heroic efforts were required to complete chemical and/or enzymatic syntheses of polysaccharides as long 92-mers. Here, we show that automated glycan assembly (AGA) enables access to a 100-mer polysaccharide via a 201-step synthesis within 188 h. Convergent block coupling of 30- and 31-mer oligosaccharide fragments, prepared by AGA, yielded a multiple-branched 151-mer polymannoside. Quick access to polysaccharides provides the basis for future material science applications of carbohydrates. |
format | Online Article Text |
id | pubmed-7304863 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-73048632020-06-22 Total Synthesis of Polysaccharides by Automated Glycan Assembly Joseph, A. Abragam Pardo-Vargas, Alonso Seeberger, Peter H. J Am Chem Soc [Image: see text] Polysaccharides are the most abundant biopolymers on earth that serve various structural and modulatory functions. Pure, completely defined linear and branched polysaccharides are essential to understand carbohydrate structure and function. Polysaccharide isolation provides heterogeneous mixtures, while heroic efforts were required to complete chemical and/or enzymatic syntheses of polysaccharides as long 92-mers. Here, we show that automated glycan assembly (AGA) enables access to a 100-mer polysaccharide via a 201-step synthesis within 188 h. Convergent block coupling of 30- and 31-mer oligosaccharide fragments, prepared by AGA, yielded a multiple-branched 151-mer polymannoside. Quick access to polysaccharides provides the basis for future material science applications of carbohydrates. American Chemical Society 2020-04-27 2020-05-13 /pmc/articles/PMC7304863/ /pubmed/32338884 http://dx.doi.org/10.1021/jacs.0c00751 Text en Copyright © 2020 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Joseph, A. Abragam Pardo-Vargas, Alonso Seeberger, Peter H. Total Synthesis of Polysaccharides by Automated Glycan Assembly |
title | Total
Synthesis of Polysaccharides by Automated Glycan
Assembly |
title_full | Total
Synthesis of Polysaccharides by Automated Glycan
Assembly |
title_fullStr | Total
Synthesis of Polysaccharides by Automated Glycan
Assembly |
title_full_unstemmed | Total
Synthesis of Polysaccharides by Automated Glycan
Assembly |
title_short | Total
Synthesis of Polysaccharides by Automated Glycan
Assembly |
title_sort | total
synthesis of polysaccharides by automated glycan
assembly |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7304863/ https://www.ncbi.nlm.nih.gov/pubmed/32338884 http://dx.doi.org/10.1021/jacs.0c00751 |
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