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Chemoenzymatic synthesis of the oligosaccharide moiety of the tumor-associated antigen disialosyl globopentaosylceramide.
- Source :
-
Organic & biomolecular chemistry [Org Biomol Chem] 2019 Aug 07; Vol. 17 (31), pp. 7304-7308. - Publication Year :
- 2019
-
Abstract
- Disialosyl globopentaosylceramide (DSGb5) is often expressed by renal cell carcinomas. To investigate properties of DSGb5, we have prepared its oligosaccharide moiety by chemically synthesizing Gb5 which was enzymatically sialylated using the mammalian sialyltransferases ST3Gal1 and ST6GalNAc5. Glycan microarray binding studies indicate that Siglec-7 does not recognize DSGb5, and preferentially binds Neu5AcĪ±(2,8)Neu5Ac containing glycans.
- Subjects :
- Antigens, Neoplasm
Carbohydrate Conformation
Enzyme Inhibitors chemistry
Globosides chemical synthesis
Globosides chemistry
HEK293 Cells
Humans
Microarray Analysis
Oligosaccharides chemistry
Sialyltransferases metabolism
beta-Galactoside alpha-2,3-Sialyltransferase
Carcinoma, Renal Cell chemistry
Enzyme Inhibitors pharmacology
Globosides pharmacology
Kidney Neoplasms chemistry
Oligosaccharides pharmacology
Sialyltransferases antagonists & inhibitors
Subjects
Details
- Language :
- English
- ISSN :
- 1477-0539
- Volume :
- 17
- Issue :
- 31
- Database :
- MEDLINE
- Journal :
- Organic & biomolecular chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 31339142
- Full Text :
- https://doi.org/10.1039/c9ob01368g