## Abstract The solution dynamics of the oligosaccharide moiety of ganglioside G~M1~ have been determined by use of a combination of ^1^H rotating frame Overhauser effect measurements and restrained molecular dynamics simulations, It is found that the GalΞ²1β3 and NeuNAc moieties which are primarily
Tryptophan fluorescence properties of cholera toxin upon interacting with ganglioside GD1b
β Scribed by M. G. Mestrallet; F. R. Bennun; B. Maggio; F. A. Cumar
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- English
- Weight
- 459 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0360-4012
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β¦ Synopsis
A blue shift of the tryptophan fluorescence emission spectra of cholera toxin or the B protomer is induced by disialoganglioside GDlb with a capacity similar to that of monosialoganglioside GM,. Both gangliosides were also capable of decreasing or reversing the fluorescence quenching by iodide ion of the toxin. The quenching constants (Ksv) for the toxin fluorescence in absence of gangliosides was 2.8 M-I; in presence of GMI or GDlb, K,, was 0.8 M-' and 0.7 M-I, respectively. Gangliosides GD,, and GTIb were unable to decrease the quenching effect. The results suggest that GDlb induces a perturbation in the tryptophan environment of the toxin molecule similar to that induced by GM I .
π SIMILAR VOLUMES
Glycosphingolipids labelled in the ceramide moiety with 3-(p-(6-phenyl)-l,3,5-hexatrienyl)phenylpropionic acid (DPH) or 6-(4nitrobenz-2-oxa-1,3-diazole-7-yl)aminohexanoic acid (NBD) were incorporated into small unilamellar lecithin liposomes. They were used in resonance energy transfer (RET) experim