Infantile, juvenile, and adult forms of G M 1 gangliosidosis have been well characterized. Certain genetic and biochemical studies have suggested that the phenotypic variation found in G,, gangliosidosis results from different allelic mutations affecting the G,, ganglioside p-galactosidase locus and
GM1 Gangliosidosis: Enzymatic variation in a single family
✍ Scribed by Dr. Donald F. Farrell; Marian P. Macmartin
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 509 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0364-5134
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Acid β‐galactosidase activity can be separated into multiple molecular forms by isoelectric focusing on cellulose acetate membranes. The residual acid β‐galactosidase in the juvenile form of G~M1~ gangliosidosis has three bands of enzyme activity with an apparent isoelectric pH (pI) range from 4.9 to 5.2, whereas that in the infantile form has a single band with an apparent isoelectric pI of 5.2. Separation of residual acid β‐galactosidase into multiple molecular forms by analytical isoelectric focusing demonstrates enzymatic differences that can be correlated with the allelic mutations that affect the G~M1~ ganglioside β‐galactosidase locus.
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