Second generation mimics of ganglioside GM1 as artificial receptors for cholera toxin: replacement of the sialic acid moiety
- 13 September 2000
- journal article
- research article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 10 (19) , 2197-2200
- https://doi.org/10.1016/s0960-894x(00)00428-5
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Carbohydrate Mimetics: A New Strategy for Tackling the Problem of Carbohydrate-Mediated Biological RecognitionAngewandte Chemie International Edition in English, 1999
- Binding of cholera toxin B-subunits to derivatives of the natural ganglioside receptor, GM1.The Journal of Biochemistry, 1999
- Structural studies of receptor binding by cholera toxin mutantsProtein Science, 1997
- AB5 toxinsCurrent Opinion in Structural Biology, 1995
- Delineation and comparison of ganglioside-binding epitopes for the toxins of Vibrio cholerae, Escherichia coli, and Clostridium tetani: evidence for overlapping epitopes.Proceedings of the National Academy of Sciences, 1994
- On the Role of the Carboxyl Group of Sialic Acid in Binding of Cholera Toxin to the Receptor Glycosphingolipid, GM11The Journal of Biochemistry, 1994
- Crystal structure of cholera toxin B‐pentamer bound to receptor GM1 pentasaccharideProtein Science, 1994
- Fuc-GM1 ganglioside mimics the receptor function of GM1 for cholera toxinBiochemistry, 1992
- Structure and function of cholera toxin and the related Escherichia coli heat-labile enterotoxin.Microbiological Reviews, 1992
- Thermodynamics of intersubunit interactions in cholera toxin upon binding to the oligosaccharide portion of its cell surface receptor, ganglioside GM1Biochemistry, 1989