i(3)so3-galactosylceramide and metaperiodate

i(3)so3-galactosylceramide has been researched along with metaperiodate* in 2 studies

Other Studies

2 other study(ies) available for i(3)so3-galactosylceramide and metaperiodate

ArticleYear
Sulfatides inhibit binding of Helicobacter pylori to the gastric cancer Kato III cell line.
    Current microbiology, 1997, Volume: 34, Issue:5

    Helicobacter pylori adhere to Kato III and Hela S3 cells in monolayer cultures. To explore whether cell surface glycoconjugates on these two cell lines mediate binding of H. pylori, various carbohydrates, glycoproteins, and glycolipids were tested to inhibit H.pylori cell adhesion. The adhesion was measured (i) with a urease-based assay and (ii) by cells stained with fluorescein. Sodium periodate and sialidase treatment (but not alpha- or beta-galactosidase, heparitinase,lysozyme, or trypsin) inhibited H. pylori binding to both cell lines. Sulfatides and sulfated glycoconjugates (50 microg/ml) but not heparin or a number of simple carbohydrates inhibited binding (1 mg/ml). The two H.pylori strains studied (CCUG 17874 and strain 25) showed high binding of soluble 125I-labeled heparin and other sulfated carbohydrate compounds.

    Topics: Bacterial Adhesion; Carbohydrate Metabolism; Glycoconjugates; HeLa Cells; Helicobacter pylori; Heparin; Humans; Neuraminidase; Periodic Acid; Stomach Neoplasms; Sulfoglycosphingolipids; Tumor Cells, Cultured

1997
Mono-sulfated globotetraosylceramide from human kidney.
    Journal of biochemistry, 1989, Volume: 106, Issue:5

    A novel sulfated glycosphingolipid that belongs to "globo-series" was isolated from human kidney. This lipid was purified from a pooled kidney preparation by chloroform-methanol extraction, mild alkaline treatment, DEAE-Sephadex and silicic acid column chromatographies, and preparative TLC. The structure and the properties were studied by IR spectroscopy, proton NMR spectroscopy, negative secondary ion-mass spectrometry, solvolysis, periodate oxidation, compositional and methylation analyses, monoclonal antibodies, and a sulfatide-binding protein. From the results of the above analyses, the structure of this glycolipid was proposed to be HSO3-3GalNAc beta 1-3Gal alpha 1-4Gal beta 1-4Glc beta 1-1ceramide. This sulfated lipid reacted with a monoclonal anti-SSEA-3 (stage-specific embryonic antigen-3) (MC-631) (Kannagi, R., Cochran, N.A., Ishigami, F., Hakomori, S., Andrews, P.W., Knowles, B.B., & Solter, D. (1983) EMBO J. 2, 2355-2361), whose epitope is R-3GalNAc beta 1-3Gal alpha 1-4Gal beta 1-R', on TLC and solid-phase radioimmunoassay. This lipid also bound to the 125I-labeled sulfatide-binding protein, thrombospondin. The yield of this sulfated glycolipid was 34 pmol/g of tissue, which was about 0.028, 0.16, and 18 mol% of galactosyl- and lactosylceramide sulfates, and globopentosylceramide sulfate (Nagai, K.-i., Roberts, D.D., Toida, T., Matsumoto, H., Kushi, Y., Handa, S., & Ishizuka, I. (1989) J. Biol. Chem. 264, in press), respectively, in human kidney.

    Topics: Animals; Antibodies, Monoclonal; Carrier Proteins; Chromatography, Thin Layer; Gas Chromatography-Mass Spectrometry; Globosides; Glycosphingolipids; Humans; Kidney; Magnetic Resonance Spectroscopy; Mass Spectrometry; Membrane Glycoproteins; Methylation; Oxidation-Reduction; Periodic Acid; Radioimmunoassay; Rats; Spectrophotometry, Infrared; Sulfoglycosphingolipids; Thrombospondins

1989