Electrophoretic analysis of glycoprotein enzymes in the sialidoses and mucolipidoses
- 1 February 1981
- journal article
- Published by Wiley in Annals of Human Genetics
- Vol. 45 (1) , 29-37
- https://doi.org/10.1111/j.1469-1809.1981.tb00303.x
Abstract
Ten enzymes, all known to be glycoproteins, were examined by electrophoresis or gel isoelectric focusing in 12 different patients with primary or secondary sialidase deficiency. Aberrant electrophoretic mobilities of many of the enzymes attributable to abnormal sialylation were found in all the patients. In ten of the patients seven of the enzymes were affected. The unaffected enzymes were beta-galactosidase, alkaline phosphatase and beta-glucuronidase. In the cells from the two patients with I cell disease (mucolipidosis II) in which sialidase is one of many deficient enzymes, beta-galactosidase, alpha-galactosidase, alpha-fucosidase and alpha-mannosidase were undetectable, alkaline phosphatase showed a normal electrophoretic mobility and acid phosphatase, adenosine deaminase, alpha-glucosidase and beta-D-N-acetylhexosaminidase showed aberrant mobilities.Keywords
This publication has 23 references indexed in Scilit:
- Successful cryopreservation of tissue and skin fibroblast cultures from patients with mucolipidosis II (I-cell disease)Cytogenetic and Genome Research, 1981
- Genetic heterogeneity in human neuraminidase deficiencyNature, 1980
- Sialidosis type 1: cherry red spot-myoclonus syndrome with sialidase deficiency and altered electrophoretic mobilities of some enzymes known to be glycoproteins. 1. Clinical findings.Journal of Neurology, Neurosurgery & Psychiatry, 1979
- Sialidosis Type 1Annals of Human Genetics, 1979
- I-cell disease: Intracellular desialylation of lysosomal enzymes using an influenza virus vectorBiochimica et Biophysica Acta (BBA) - General Subjects, 1979
- Neonatal presentation of I-cell diseaseThe Journal of Pediatrics, 1978
- Neuraminidase deficiency in the cherry red spot-myoclonus syndromeBiochemical and Biophysical Research Communications, 1977
- Genetic heterogeneity in GM1-gangliosidosisNature, 1975
- ANGIOKERATOMA CORPORIS DIFFUSUM AND LYSOSOMAL ENZYME DEFICIENCYThe Lancet, 1974
- Differences between the N‐acetyl hexosaminidase isozymes in serum and tissuesAnnals of Human Genetics, 1974