Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (8)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Roche, N.
Right arrow Articles by Teneberg, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Roche, N.
Right arrow Articles by Teneberg, S.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Glycobiology, 2001, Vol. 11, No. 11 935-944
© 2001 Oxford University Press

Helicobacter pylori–binding gangliosides of human gastric adenocarcinoma

Niamh Roche1, Thomas Larsson, Jonas Ångström and Susann Teneberg

Institute of Medical Biochemistry, Göteborg University, P.O. Box 440, SE 405 30 Göteborg, Sweden

Acidic and neutral glycosphingolipids were isolated from a human gastric adenocarcinoma, and binding of Helicobacter pylori to the isolated glycosphingolipids was assessed using the chromatogram binding assay. The isolated glycosphingolipids were characterized using fast atom bombardment mass spectrometry and by binding of antibodies and lectins. The predominating neutral glycosphingolipids were found to migrate in the di- to tetraglycosylceramide regions as revealed by anisaldehyde staining and detection with lectins. No binding of H. pylori to these compounds was obtained. The most abundant acidic glycosphingolipids, migrating as the GM3 ganglioside and sialyl-neolactotetraosylceramide, were not recognized by the bacteria. Instead, H. pylori selectively interacted with slow-migrating, low abundant gangliosides not detected by anisaldehyde staining. Binding-active gangliosides were isolated and characterized by mass spectrometry, proton nuclear magnetic resonance, and lectin binding as sialyl-neolactohexaosylceramide (NeuAc{alpha}3Galß4GlcNAcß3Galß4GlcNAcß3Galß4Glcß1Cer) and sialyl-neolactooctaosylceramide (NeuAc{alpha}3Galß4GlcNAcß3Galß4GlcNAcß3Galß4GlcNAcß3Galß4Glcß1Cer).

1 To whom correspondence should be addressed


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
GlycobiologyHome page
A. Gustafsson, A. Hultberg, R. Sjostrom, I. Kacskovics, M. E. Breimer, T. Boren, L. Hammarstrom, and J. Holgersson
Carbohydrate-dependent inhibition of Helicobacter pylori colonization using porcine milk
Glycobiology, January 1, 2006; 16(1): 1 - 10.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
M. Unemo, M. Aspholm-Hurtig, D. Ilver, J. Bergstrom, T. Boren, D. Danielsson, and S. Teneberg
The Sialic Acid Binding SabA Adhesin of Helicobacter pylori Is Essential for Nonopsonic Activation of Human Neutrophils
J. Biol. Chem., April 15, 2005; 280(15): 15390 - 15397.
[Abstract] [Full Text] [PDF]


Home page
Infect. Immun.Home page
N. Roche, J. Angstrom, M. Hurtig, T. Larsson, T. Boren, and S. Teneberg
Helicobacter pylori and Complex Gangliosides
Infect. Immun., March 1, 2004; 72(3): 1519 - 1529.
[Abstract] [Full Text] [PDF]


Home page
GlycobiologyHome page
H. Miller-Podraza, P. Johansson, J. Angstrom, T. Larsson, M. Longard, and K.-A. Karlsson
Studies on gangliosides with affinity for Helicobacter pylori: binding to natural and chemically modified structures
Glycobiology, March 1, 2004; 14(3): 205 - 217.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.