Semi-synthesis of chondroitin sulfate-E from chondroitin sulfate-A.

Carbohydr Polym

Department of Chemistry and Chemical Biology, Center for Biotechnology and Interdisciplinary Studies, Rensselaer Polytechnic Institute, Troy, New York 12180, USA.

Published: January 2012

Chondroitin sulfate-E (chondroitin-4, 6-disulfate) was prepared from chondroitin sulfate-A (chondroitin-4 - sulfate) by regioselective sulfonation, performed using trimethylamine sulfur trioxide in formamide under argon. The structure of semi-synthetic chondroitin sulfate-E was analyzed by PAGE, (1)H NMR, (13)C NMR, 2D NMR and disaccharide analysis and compared with natural chondroitin sulfate-E. Both semi-synthetic and natural chondroitin sulfate-E were each biotinylated and immobilized on BIAcore SA biochips and their interactions with fibroblast growth factors displayed very similar binding kinetics and binding affinities. The current semi-synthesis offers an economical approach for the preparation of the rare chondroitin sulfate-E from the readily available chondroitin sulfate-A.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3225962PMC
http://dx.doi.org/10.1016/j.carbpol.2011.08.075DOI Listing

Publication Analysis

Top Keywords

chondroitin sulfate-e
24
chondroitin sulfate-a
12
chondroitin
8
sulfate-e chondroitin
8
natural chondroitin
8
sulfate-e
6
semi-synthesis chondroitin
4
sulfate-a chondroitin
4
sulfate-e chondroitin-4
4
chondroitin-4 6-disulfate
4

Similar Publications

Article Synopsis
  • Researchers developed a green enzymatic method to produce chondroitin sulfate E (CSE) from chondroitin sulfate A (CSA), which helps avoid contamination issues linked with animal-derived products.
  • They identified and engineered a sulfotransferase enzyme, CHST15, boosting its efficiency in converting CSA to CSE by 3.5 times.
  • A six-enzyme whole-cell catalyst was created, achieving a 72.2% conversion of CSA to CSE within 24 hours, highlighting a sustainable approach for industrial CSE production.
View Article and Find Full Text PDF

Chondroitin sulfate E (CS-E) is a vital sulfated glycosaminoglycan with diverse biological functions and therapeutic potential. This study marks a significant milestone by achieving the first successful microbial production of chondroitin 4-sulfate 6-O-sulfotransferase (GalNAc4S-6ST) in Escherichia coli, enabling recombinant CS-E biosynthesis. Initially, we identified sulfotransferases capable of converting chondroitin sulfate A (CS-A) to CS-E, but these enzymes were non-functional when expressed in E.

View Article and Find Full Text PDF

Inhibition of Astrocytic Carbohydrate Sulfotransferase 15 Promotes Nerve Repair After Spinal Cord Injury via Mitigation of CSPG Mediated Axonal Inhibition.

Cell Mol Neurobiol

August 2023

Key Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao, 266071, China.

Nerve tissue regeneration is a significant problem. After neural diseases and damage such as spinal cord injury (SCI), the accumulation of chondroitin sulfate proteoglycans (CSPG) comprising axonal inhibitory glycosaminoglycan chains in the microenvironment is a major barrier that obstructs nerve repair. Interfering with the production of glycosaminoglycans, especially the critical inhibitory chains, could be a potential therapeutic strategy for SCI, which is, however, poorly defined.

View Article and Find Full Text PDF
Article Synopsis
  • Glycosaminoglycans (GAGs) are polysaccharides on cell surfaces, playing key roles in growth factor signaling, with variations in their sulfation impacting function.
  • The study focused on cochlins, proteins that bind sulfated GAGs, using a recombinant cochlin to identify specific binding to heparan sulfate and chondroitin sulfate E.
  • By analyzing cochlin mutants, the research developed a GAG detection system, revealing that the N-terminal of cochlin is crucial for binding, which may advance understanding of disease mechanisms related to GAG modifications.
View Article and Find Full Text PDF

O-sulfated N-acetyl-d-galactosamine (GalNAc) residues in chondroitin sulfate (CS) play a crucial role in chondroitinase ABC I (cABC-I) activity. CSA containing mainly 4-O-monosulfated GalNAc was a good substrate for the enzyme, but not CSE containing mainly 4,6-O-disulfated GalNAc [GalNAc(4S,6S)]. Each CS isomer exhibits structural heterogeneity; CSE has di-sulfated disaccharide units and mono-sulfated disaccharide units.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!