IP Library › Granted Patent US 11,530,393
Granted Patent B2
US 11,530,393 · App. 17/092,034 · Granted Dec 20, 2022

Compositions comprising iduronate-2-sulfatase

Inventor: Dave Nichols (Lexington, MA)
Assignee: TAKEDA PHARMACEUTICAL COMPANY LIMITED
C12N9/16A61K38/465C12Y301/06013
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Quick Facts
Patent No.
US 11,530,393
App. No.
17/092,034
Granted
Dec 20, 2022
Kind
B2
Abstract

The present invention provides, among other things, improved methods for purifying I2S protein produced recombinantly for enzyme replacement therapy. The present invention is, in part, based on the surprising discovery that recombinant I2S protein can be purified from unprocessed biological materials, such as, I2S-containing cell culture medium, using a process involving as few as four chromatography columns.

Claims (25)

1. A composition comprising purified recombinant iduronate-2-sulfatase (I2S) having an amino acid sequence at least 90% identical to SEQ ID NO:1,

wherein the purified recombinant I2S comprises at least 70% conversion of the cysteine residue corresponding to Cys59 of SEQ ID NO:1 to Cα-formylglycine (FGly),

wherein the purified recombinant I2S comprises on average at least 16 sialic acids per molecule; and

wherein the purified recombinant I2S has specific activity of at least 20 U/mg as determined by an in vitro 4-MUF-SO4 to 4-MUF conversion assay.

2. The composition of claim 1 , wherein the purified recombinant I2S comprises a moiety that binds to a receptor on the surface of target cells.

3. The composition of claim 2 , wherein the moiety that binds to a receptor on the surface of a target cell is fused to the recombinant I2S at the N-terminus, C-terminus, or internally.

4. The composition of claim 1 , wherein the purified recombinant I2S comprises on average at least 18 sialic acids per molecule.

5. The composition of claim 1 , wherein the purified recombinant I2S protein has a specific activity of at least 30 U/mg as determined by an in vitro 4-MUF-SO 4 to 4-MUF conversion assay.

6. The composition of claim 1 , wherein the purified recombinant I2S protein has a specific activity of at least 40 U/mg as determined by an in vitro 4-MUF-SO 4 to 4-MUF conversion assay.

7. The composition of claim 1 , wherein the purified recombinant I2S protein has a specific activity of at least 50 U/mg as determined by an in vitro 4-MUF-SO 4 to 4-MUF conversion assay.

8. The composition of claim 1 , wherein the purified recombinant I2S protein has a specific activity of at least 60 U/mg as determined by an in vitro 4-MUF-SO 4 to 4-MUF conversion assay.

9. The composition of claim 1 , wherein the purified recombinant I2S contains at least 20% bis-phosphorylated oligosaccharides per molecule.

10. The composition of claim 1 , wherein the purified recombinant I2S contains at least 50% bis-phosphorylated oligosaccharides per molecule.

11. A composition comprising purified recombinant iduronate-2-sulfatase (I2S) having an amino acid sequence at least 90% identical to SEQ ID NO:1,

wherein the purified recombinant I2S comprises at least 70% conversion of the cysteine residue corresponding to Cys59 of SEQ ID NO:1 to Cα-formylglycine (FGly),

wherein the purified recombinant I2S comprises on average at least 16 sialic acids per molecule; and

wherein the purified recombinant I2S has specific activity of at least 40 U/mg as determined by an in vitro sulfate release activity assay using heparin disaccharide as substrate.

12. The composition of claim 11 , wherein the purified recombinant I2S comprises a moiety that binds to a receptor on the surface of target cells.

13. The composition of claim 12 , wherein the moiety that binds to a receptor on the surface of a target cell is fused to the recombinant I2S at the N-terminus, C-terminus, or internally.

14. The composition of claim 11 , wherein the purified recombinant I2S protein has specific activity of at least 50 U/mg as determined by an in vitro sulfate release activity assay using heparin disaccharide as substrate.

15. The composition of claim 11 , wherein the purified recombinant I2S protein has specific activity of at least 60 U/mg as determined by an in vitro sulfate release activity assay using heparin disaccharide as substrate.

16. The composition of claim 11 , wherein the purified recombinant I2S contains at least 20% bis-phosphorylated oligosaccharides per molecule.

17. The composition of claim 11 , wherein the purified recombinant I2S contains at least 50% bis-phosphorylated oligosaccharides per molecule.

18. The composition of claim 1 , wherein the purified recombinant I2S has an amino acid sequence identical to SEQ ID NO:1.

19. The composition of claim 11 , wherein the purified recombinant I2S has an amino acid sequence identical to SEQ ID NO:1.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 15, 2022
From: SHIRE HUMAN GENETIC THERAPIES, INC.
To: TAKEDA PHARMACEUTICAL COMPANY LIMITED
Reel/Frame 061447/0760 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 18, 2022
From: NICHOLS, DAVE
To: SHIRE HUMAN GENETIC THERAPIES, INC.
Reel/Frame 059314/0391 →
Continuity (6)
Continuation 16417440 · May 20, 2019
Division 15279018 · Sep 28, 2016
Division 14673607 · Mar 30, 2015
Division 13829706 · Mar 14, 2013
Provisional Application 61666733 · Jun 29, 2012
Related Publication 20210317426A1 · Oct 14, 2021
Cited By (1)
US 12,359,178