GAGs are highly negatively charged linear polysaccharides. It consists mainly of disaccharide repeats composed of glucose or galactose and hexane-dioic acid. CD BioGlyco has developed different structures of GAG array on cells such as chondroitin sulfate (CS), dermatan sulfate (DS), heparin sulfate (HS), heparin (HP), and keratan sulfate (KS). More than 40 glycosyltransferases, epimerases, sulfotransferases, and other enzymes are involved in the biosynthesis of GAGs. We provide modification services such as sulfation, N-acetylation, and differential isomerization. Meanwhile, utilizing the ability of cells to carry out GAG biosynthesis, our researchers produce and display GAG on a cell-based array and interrogate the detailed structural features required for specific biological activities.
Fig.1 Schematic diagram of cell-based GAG array service. (CD BioGlyco)
Paper Title: The GAGOme: a cell-based library of displayed glycosaminoglycans
Technology: RNA sequencing, High-performance liquid chromatography (HPLC), Gene editing, Flow cytometry
Journal: Nature Methods
Published: 2018
IF: 47.99
Results: In this paper, a gene-targeted gRNA library was developed to extend the GAGOme library. A more comprehensive GAG library was constructed from cell lysates or by recombinantly expressed proteoglycans, which was further used to generate cell-based arrays to display and study the biological functions of GAGs. Further refinement of epitope recognition and identification of biosynthetic and genetic bases was achieved by displaying different distinct protein-bound GAGs through the GAGOme library.
Fig.2 Predicted GAG biosynthetic capabilities of WT CHO and HEK293 cells based on RNAseq analysis. (Chen, et al., 2018)
CD BioGlyco has professional operators and sophisticated high-throughput analytical instruments to provide satisfactory service. Our Glycan Display Platform provides a comprehensive service for clients. If you want to know more information, please feel free to contact us.
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