Stimulation of GM3 ganglioside sialidase activity by an activator protein in patients with mucolipidosis IV and controls
- PMID: 1806363
- DOI: 10.1159/000468861
Stimulation of GM3 ganglioside sialidase activity by an activator protein in patients with mucolipidosis IV and controls
Abstract
An activator protein that stimulates the enzymic hydrolysis of sialic acid from gangliosides by ganglioside sialidase was fractionated from human liver. This fraction was distinct from those stimulating the hydrolysis of galactose from GM1 ganglioside by beta-galactosidase and the hydrolysis of N-acetylgalactosamine from GM2 ganglioside by hexosaminidase A. This fraction was highly specific for the hydrolysis of sialic acid from GM3 ganglioside, and was equally effective in fibroblasts from patients with mucolipidosis IV and in fibroblasts from controls.
Similar articles
-
Ganglioside GM3 sialidase activity in fibroblasts of normal individuals and of patients with sialidosis and mucolipidosis IV. Subcellular distribution and and some properties.Biochem J. 1989 May 15;260(1):69-74. doi: 10.1042/bj2600069. Biochem J. 1989. PMID: 2775195 Free PMC article.
-
Evidence for sialidase hydrolyzing gangliosides GM2 and GM1 in rat liver plasma membrane.FEBS Lett. 1986 Oct 6;206(2):223-8. doi: 10.1016/0014-5793(86)80985-1. FEBS Lett. 1986. PMID: 3758350
-
The sialic acid residue of exogenous GM1 ganglioside is recycled for biosynthesis of sialoglycoconjugates in rat liver.Biochem J. 1987 Oct 1;247(1):157-64. doi: 10.1042/bj2470157. Biochem J. 1987. PMID: 3689344 Free PMC article.
-
Catalytically defective ganglioside neuraminidase in mucolipidosis IV.Clin Genet. 1982 Jun;21(6):374-81. doi: 10.1111/j.1399-0004.1982.tb01390.x. Clin Genet. 1982. PMID: 6813002
-
Metabolism of ganglioside-amides in cultured human fibroblasts.Biol Chem Hoppe Seyler. 1987 Nov;368(11):1495-503. doi: 10.1515/bchm3.1987.368.2.1495. Biol Chem Hoppe Seyler. 1987. PMID: 3124867