Methods for introducing mannose 6-phosphate and other oligosaccharides onto glycoproteins and its application thereof
Methods to introduce highly phosphorylated mannopyranosyl oligosaccharide derivatives containing mannose-6-phosphate (M6P), or other oligosaccharides bearing other terminal hexoses, to carbonyl groups on oxidized glycans of glycoproteins while retaining their biological activity are described. The methods are useful for modifying glycoproteins, including those produced by recombinant protein expression systems, to increase uptake by cell surface receptor-mediated mechanisms, thus improving their therapeutic efficacy in a variety of applications.
1. A modified lysosomal enzyme comprising a glycosylated lysosomal enzyme coupled to a biantennary oligosaccharide comprising:
wherein M is mannose or a mannopyranosyl group and P is a phosphate group.
2. The modified lysosomal enzyme of claim 1 , wherein the oligosaccharide is coupled to the glycosylated lysosomal enzyme through a carbon-nitrogen double bond.
3. The modified lysosomal enzyme of claim 2 , wherein the carbon-nitrogen double bond is formed by reacting a carbonyl group on the glycosylated lysosomal enzyme with a carbonyl-reactive group on the oligosaccharide.
4. The modified lysosomal enzyme of claim 3 , wherein the carbonyl-reactive group is chosen from a hydrazine, a hydrazide, an aminooxy, and a semicarbazide.
5. The modified lysosomal enzyme of claim 4 , wherein the carbonyl-reactive group is aminooxy.
6. The modified lysosomal enzyme of claim 1 , wherein the core mannose is attached to a linker through a β1 linkage.
7. The modified lysosomal enzyme of claim 1 , wherein the lysosomal enzyme is acid alpha-glucosidase.
8. The modified lysosomal enzyme of claim 1 , prepared by
(a) derivatizing the biantennary oligosaccharide comprising a phosphorylated mannose with a compound containing a carbonyl-reactive group;
(b) oxidizing at least one glycan on the glycosylated lysosomal enzyme to generate at least one carbonyl group; and
(c) reacting the carbonyl-reactive group on the oligosaccharide with the carbonyl group on the glycosylated lysosomal enzyme,
thereby coupling the oligosaccharide to the lysosomal enzyme.
9. The modified lysosomal enzyme of claim 8 , wherein the carbonyl-reactive group is chosen from a hydrazine, a hydrazide, an aminooxy, and a semicarbazide.
10. The modified lysosomal enzyme of claim 9 , wherein the carbonyl-reactive group is an aminooxy.
11. A composition comprising the modified lysosomal enzyme of claim 1 .
12. A modified lysosomal enzyme comprising a glycosylated lysosomal enzyme coupled to a biantennary oligosaccharide comprising:
wherein M is mannose or a mannopyranosyl group and P is a phosphate group.
13. A composition comprising the modified lysosomal enzyme of claim 12 .
14. The composition of claim 13 , wherein the lysosomal enzyme is acid alpha-glucosidase.
15. A biantennary oligosaccharide comprising:
wherein R is a chemical group containing at least one carbonyl-reactive group.
16. The oligosaccharide of claim 15 , wherein the at least one carbonyl-reactive group is chosen from a hydrazine, a hydrazide, an aminooxy, and a semicarbazide.
17. The oligosaccharide of claim 15 , wherein R contains a hydrazine and an aminooxy.
18. A modified lysosomal enzyme comprising a glycosylated lysosomal enzyme coupled to the oligosaccharide of claim 17 .
19. The modified lysosomal enzyme of claim 18 , wherein the lysosomal enzyme is acid alpha-glucosidase.
20. A biantennary compound having the formula:
wherein R is a chemical group containing at least one carbonyl-reactive group.
21. A biantennary oligosaccharide comprising:
wherein M is mannose or a mannopyranosyl group and P is a phosphate group.
22. A biantennary compound having the formula:
wherein M is mannose or a mannopyranosyl group and P is a phosphate group.