HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Pathogenesis of shigella diarrhea: evidence for an N-linked glycoprotein shigella toxin receptor and receptor modulation by beta-galactosidase.

Abstract
Pathogenic mechanisms in infectious diseases often involve specific receptor-ligand interactions of cells and soluble molecules. To further elucidate structure-function relations for shigella toxin receptors, we studied binding of purified 125I-labeled toxin and biologic response under various conditions in an experimental model using HeLa cells. Response to toxin was reversibly inhibited by treatment of cells with trypsin or tunicamycin, an inhibitor of glycoprotein synthesis that also significantly inhibited toxin binding, a result indicating that the receptor is an N-linked glycoprotein. Removal of terminal beta-linked galactose from the HeLa cell surface with beta-galactosidase increased toxin binding and activity, and it also potentiated the effects of lysozyme and wheat-germ agglutinin, which recognize oligomeric beta 1----4-linked N-acetyl-D-glucosamine and inhibit toxin activity as well. Incubation of cells with beta-N-acetylglucosaminidase, which cleaves terminal beta-linked N-acetyl-D-glucosamine, inhibited toxin activity. Effects of beta-galactosidase were reversed by readdition of galactose to cell-surface oligosaccharide acceptors. The data demonstrate that alterations of a single sugar on cell-surface glycoproteins may have a dramatic effect on receptor activity and indicate that shigella toxin is a sugar-binding protein with specificity for beta 1----4-linked N-acetyl-D-glucosamine.
AuthorsG T Keusch, M Jacewicz, A Donohue-Rolfe
JournalThe Journal of infectious diseases (J Infect Dis) Vol. 153 Issue 2 Pg. 238-48 (Feb 1986) ISSN: 0022-1899 [Print] United States
PMID3003205 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Bacterial Toxins
  • Glycoproteins
  • Lectins
  • Receptors, Cell Surface
  • Receptors, Immunologic
  • Shiga Toxins
  • Wheat Germ Agglutinins
  • shigella toxin receptor
  • Tunicamycin
  • Galactosidases
  • Muramidase
  • Neuraminidase
  • alpha-Galactosidase
  • beta-Galactosidase
  • Trypsin
  • Acetylglucosamine
  • Galactose
Topics
  • Acetylglucosamine (metabolism)
  • Bacterial Toxins (metabolism, toxicity)
  • Cell Survival
  • Dysentery, Bacillary (microbiology)
  • Galactose (pharmacology)
  • Galactosidases (pharmacology)
  • Glycoproteins (metabolism)
  • HeLa Cells
  • Humans
  • Lectins (pharmacology)
  • Muramidase (pharmacology)
  • Neuraminidase (pharmacology)
  • Receptors, Cell Surface
  • Receptors, Immunologic (analysis, metabolism)
  • Shiga Toxins
  • Trypsin (pharmacology)
  • Tunicamycin (pharmacology)
  • Wheat Germ Agglutinins
  • alpha-Galactosidase (pharmacology)
  • beta-Galactosidase (pharmacology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: