Abstract
I-cell disease (mucolipidosis II) is presented as a model for endo- and exo-cytosis phenomena in man. A hypothesis is presented for the structure of the carbohydrate recognition site on fibroblast-derived β-D-N-acetylhexosaminidase that may extend to the other affected hydrolases and that is responsible for specific uptake of the enzyme by fibroblasts. The proposed neuraminidase deficiency in I-cell disease is discussed in the light of its significance in influencing the final sugar sequence in the carbohydrate structure of the recognition site.
| Original language | English |
|---|---|
| Pages (from-to) | 509-512 |
| Number of pages | 4 |
| Journal | Biochemical Journal |
| Volume | 171 |
| Issue number | 2 |
| DOIs | |
| State | Published - 1978 |
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