Glycosylation- and phosphorylation-dependent intracellular transport of lysosomal hydrolases.

Abstract

Lysosomes contain more than 50 soluble hydrolases that are targeted to lysosomes in a mannose 6-phosphate (Man6P)-dependent manner. The phosphorylation of man- nose residues on high mannose-type oligosaccharides of newly synthesized lysosomal enzymes is catalyzed by two multimeric enzymes, GlcNAc-1-phosphotransferase and GlcNAc-1-phosphodiester-alpha-N-acetylglucosaminidase, allowing the binding to two distinct Man6P receptors in the Golgi apparatus. Inherited defects in the GlcNAc-1-phosphotransferase complex result in missorting and cellular loss of lysosomal enzymes, and the subsequent lysosomal dysfunction causes the lysosomal storage disorders mucolipidosis types II and III. Biosynthetic studies and the availability of Man6P receptor-deficient mouse models have provided new insights into the structural requirements for preferential binding of subsets of lysosomal enzymes to Man6P receptors as well as the identification of alternative targeting pathways.

• Authors: Sandra Pohl, Katrin Marschner, Stephan Storch, Thomas Braulke
• Journal: Biological chemistry (Biol Chem) Vol. 390 Issue 7 Pg. 521-7 (Jul 2009) ISSN: 1431-6730 [Print] Germany
• PMID: 19426136 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)

Chemical References

• Hydrolases

Topics

• Animals
• Glycosylation
• Humans
• Hydrolases (biosynthesis, metabolism)
• Intracellular Space (metabolism)
• Lysosomes (enzymology)
• Phosphorylation
• Protein Transport