J. Lipid Res. Did you know there is a large type edition? Click here.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ulrich-Bott, B.
Right arrow Articles by Wiegandt, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ulrich-Bott, B.
Right arrow Articles by Wiegandt, H.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

Journal of Lipid Research, Vol 25, 1233-1245, Copyright © 1984 by Lipid Research, Inc.


ARTICLES

Micellar properties of glycosphingolipids in aqueous media

B Ulrich-Bott and H Wiegandt

The aggregation properties of neutral glycosphingolipids and gangliosides were investigated by ultracentrifugal sedimentation and gel permeation chromatography. Initially, glycosphingolipids in buffer formed high molecular aggregates. On standing, the glycosphingolipids produced smaller and stable micelles in equilibrium with their monomers at the critical micellar concentration (cmc). The cmc's of monohexaosyl- to tetrahexaosylceramides were on the order of 10(-8) to 10(-7)M. In contrast, values of 10(-8)M for monosialogangliosides and 10(-6)-10(- 5)M for di- and trisialogangliosides were found. From estimations of hydrodynamic radii, Svedberg coefficients, and partial specific volumes, relative masses of glycosphingolipid micelles were calculated to be in the range of 300 to 1000 for the neutral glycosphingolipids and 100 to 350 for the gangliosides.
Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
J AndrolHome page
M. Gavella, M. Kveder, V. Lipovac, R. Rakos, and G. Pifat
Trisialoganglioside GT1b Prevents Increase in Sperm Membrane Molecular Ordering Induced by In Vitro Lipid Peroxidation
J Androl, November 1, 2005; 26(6): 724 - 731.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
M. L. Malakhova, L. Malinina, H. M. Pike, A. T. Kanack, D. J. Patel, and R. E. Brown
Point Mutational Analysis of the Liganding Site in Human Glycolipid Transfer Protein: FUNCTIONALITY OF THE COMPLEX
J. Biol. Chem., July 15, 2005; 280(28): 26312 - 26320.
[Abstract] [Full Text] [PDF]


Home page
Mol. Biol. CellHome page
M. Rusnati, E. Tanghetti, C. Urbinati, G. Tulipano, S. Marchesini, M. Ziche, and M. Presta
Interaction of Fibroblast Growth Factor-2 (FGF-2) with Free Gangliosides: Biochemical Characterization and Biological Consequences in Endothelial Cell Cultures
Mol. Biol. Cell, February 1, 1999; 10(2): 313 - 327.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 All ASBMB Journals   Journal of Biological Chemistry 
 Molecular and Cellular Proteomics   ASBMB Today 
Copyright © 1984 by the American Society for Biochemistry and Molecular Biology.