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ganglioside analysis cyberlipid.org |
Ganglioside is a compound composed of a glycosphingolipid (ceramide and oligosaccharide) with one or more sialic acids (AKA n-acetylneuraminic acid, NANA) linked on the sugar chain. The 60+ known gangliosides differ mainly in the position and number of NANA residues. It is a component of the cell plasma membrane that modulates cell signal transduction events. It appears that they concentrate in lipid rafts. They have recently been found to be highly important in immunology. Natural and semisynthetic gangliosides are considered possible therapeutics for neurodegenerative disorders.[1] Gangliosides are more complex glycosphingolipids in which oligosaccharide chains containing N-acetylneuraminic acid (NeuNAc) are attached to a ceramide. NeuNAc, an acetylated derivative of the carbohydrate sialic acid, makes the head groups of Gangliosides anionic. NB: the M in GM2 stands for monosialo, i.e., one NeuNAc residue. GM2 is the second monosialo ganglioside characterized, thus the subscript 2. Their structural diversity results from variation in the composition and sequence of the sugar residues. In all Gangliosides, the ceramide is linked through its C-1 to a β-glucosyl residue, which, in turn, is bound to a β-galactosyl residue. The name ganglioside was first applied by the German scientist Ernst Klenk in 1942 to lipids newly isolated from ganglion cells of brain [2]
[edit] LocationThey are present on cell surfaces, with the 2 hydrocarbon chains of the ceramide moiety embedded in the plasma membrane and the oligosaccharides on the extracellular surface. They are found predominantly in the nervous system where they constitute 6% of all phospholipids. They are involved in diverse roles including cell-to-cell contact, ion conductance, and receptor. [edit] FunctionGangliosides, glycosphingolipids, and glycoproteins found on the surface of oligosaccharide provide cells with distinguishing surface markers that can serve in cellular recognition and cell-to-cell communication. Structures similar to the ABO blood group antigens on the surface of human cells can be oligosaccharide components of glycosphingolipids in addition to being linked to proteins to form glycoproteins. [edit] Common gangliosides
[edit] structures of the common gangliosidesGM2-1 = aNeu5Ac(2-3)bDGalp(1-?)bDGalNAc(1-?)bDGalNAc(1-?)bDGlcp(1-1)Cer where [edit] Pathobiology[edit] GangliosidosesMutations in genes coding for enzymes of ganglioside metabolism cause severe lipid storage diseases called gangliosidoses, that encomprise GM1 gangliosidosis and GM2 gangliosidosis (Tay-Sachs Disease and Sandhoff disease). The non-functioning beta-galactosidase (GM1) or hexosaminidase (GM2) causes the accumulation of gangliosides in lysososmes (lysosomal storage disease) of several cells (macrophages, neurons), disturbing their functions. [edit] MiscellaneousGanglioside are also involved in several diseases:
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