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PMID: 3081038 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Biosynthesis of the sulfatide/GM1 activator protein (SAP-1) in control and mutant cultured skin fibroblasts.

Biochimica et biophysica acta ·Vol. 875 ·No. 3 ·1986-02-28 ·Pages 554-62

Fujibayashi S, Wenger DA

Abstract

Sphingolipid activator proteins (SAP) are relatively low-molecular-mass proteins that stimulate the hydrolysis of specific sphingolipids by the required lysosomal enzymes. SAP-1 or sulfatide/GM1 ganglioside activator protein has previously been demonstrated to stimulate the enzymatic hydrolysis of sulfatide, GM1 ganglioside and globotriaosylceramide. Using monospecific rabbit antibodies against human liver sulfatide/GM1 activator, the biosynthesis and processing of this activator were studied in cultured skin fibroblasts from controls and patients with GM1 gangliosidosis and a variant form of metachromatic leukodystrophy. When [35S]methionine was presented in the medium to control human fibroblasts for 4 h, the majority of the immunoprecipitable radiolabeling was confined to bands within three regions of apparent molecular mass 65-70, 35-52 and 8-13 kDa. The only immunoprecipitable radiolabeled species excreted into the medium when NH4Cl was present had an apparent molecular mass of 70 kDa. When the excretion products were given to fresh cells followed by incubation for up to 24 h there was production of the mature species. Treatment of the 70 kDa form with endoglycosidase F resulted in production of a 53 kDa molecular mass form. Pulse-chase experiments indicated that the initial immunoprecipitable translation product was 65 kDa which increased to 70 kDa over the next hour. The 65 kDa species must result from co-translational glycosylation of the polypeptide chain. Apparently, intralysosomal processing converts the 13 kDa form to the 8-11 kDa species. The cells from the patient with GM1 gangliosidosis could not process to the smallest species found in controls due to the deficiency of acid beta-galactosidase. Patients who have a variant form of metachromatic leukodystrophy do not make any immunoprecipitable radiolabeled products in the cells or in the media. This indicates a severe mutation in the gene coding for this activator protein. The production of such small mature species from a relatively large precursor form may regulate the production of this interesting protein.

MeSH Terms
Cells, Cultured Electrophoresis, Polyacrylamide Gel Endocytosis Fibroblasts/metabolism G(M1) Ganglioside Gangliosidoses/metabolism Glycoproteins Glycoside Hydrolases Humans Immunochemistry Leukodystrophy, Metachromatic/metabolism Mannosyl-Glycoprotein Endo-beta-N-Acetylglucosaminidase Methionine/metabolism Mucolipidoses/metabolism Mutation Photofluorography Protein Biosynthesis Proteins/genetics,metabolism Saposins Sphingolipid Activator Proteins
Chemicals
Glycoproteins PSAP protein, human Proteins Saposins Sphingolipid Activator Proteins G(M1) Ganglioside Methionine Glycoside Hydrolases Mannosyl-Glycoprotein Endo-beta-N-Acetylglucosaminidase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Fujibayashi S
Wenger D A
Article Info
Journal
Biochimica et biophysica acta
Abbr.
Biochim Biophys Acta
ISSN
0006-3002
Published
1986-02-28
Pages
554-62
Language
English
Region
Netherlands
NLM ID
0217513
Subset
IM
Grants
NIADDK NIH HHS · AM 33170 · United States
NICHD NIH HHS · HD 08315 · United States
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