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Isolation of three novel cholinergic neuron-specific gangliosides from bovine brain and theirin vitro syntheses
Authors:Fumitoshi Irie  Sadamu Kurono  Yu-Teh Li  Yousuke Seyama  Yoshio Hirabayashi
Institution:1. Laboratory for Cellular GlycoBiology, Frontier Research Program, The Institute of Physical and Chemical Research (RIKEN), Hirosawa, Wako-shi, 351-01, Saitama, Japan
2. Department of Physiological Chemistry and Nutrition, Faculty of Medicine, The University of Tokyo, Hongo, Bunkyo-ku, 113, Tokyo, Japan
3. Department of Biochemistry, Tulane University School of Medicine, 70112, New Orleans, Louisiana, USA
Abstract:In the present study, three extremely minor but novel Chol-1 antigens, termed X1, X2, and X3 have been isolated from bovine brain gangliosides. Based on the results of sialidase degradation, TLC-immunostaining with anti-Chol-1 antibody and fast atom bombardment mass spectrometry, their chemical structures were identified as: $$\begin{gathered} III^6 NeuAc--GgOse4Cer (X1:GM1\alpha ) \hfill \\ III^6 NeuAc,II^3 NeuAc--GgOse4Cer (X2:GT1a\alpha ) \hfill \\ III^6 NeuAc,II^3 NeuAc--NeuGc--GgOse4Cer (X3:GT1b\alpha ) \hfill \\ \end{gathered} $$ The yields of GM1α, GD1aα, and GT1bα, were approximately 150, 20, and 10 µg, respectively, from 10 g of the bovine brain ganglioside mixture. In conjunction with our previous observations, all gangliosides with anti-Chol-1 reactivity were found to contain a common sialyl α2–6N-acetylgalactosamine residue, indicating that this unique sialyl linkage is the specific antigenic determinant. We subsequently examined the biosyntheses of the three novel Chol-1 gangliosides using rat liver Golgi fraction as an enzyme source. The results showed that GM1α, GD1aα, and GT1bα were synthesized from asialo-GM1, GM1a, and GD1b, respectively, by the action of a GalNAc α2-6sialyltransferase.
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