IP Library Granted Patent US 8,834,866
Granted Patent B2
US 8,834,866 · App. 13/378,283 · Granted Sep 16, 2014

Methods and compositions for treatment of myotubular myopathy using chimeric polypeptides comprising myotubularin 1(MTM1) polypeptides

Inventor: Dustin D. Armstrong (Everett, MA)
Assignee: Valerion Therapeutics, LLC
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Quick Facts
Patent No.
US 8,834,866
App. No.
13/378,283
Granted
Sep 16, 2014
Kind
B2
Abstract

The present invention provides chimeric polypeptides comprising myotubularin 1 (MTMI) polypeptides and an internalising moiety, wherein, the moiety can be an antibody, and is preferably monoclonal antibody 3E10, a functional variant or a fragment thereof. One aspect of the present invention provides compositions comprising these chimeric polypeptides together with a pharmaceutically acceptable carrier, and optionally, a further therapeutic agent. Another aspect of the present invention provides methods of treating Myotubular Myopathy comprising administering the polypeptides or compositions comprising the polypeptides to a subject in need.

Claims (28)

1. A chimeric polypeptide comprising: (i) a myotubularin (MTM1 ) polypeptide, or a bioactive fragment thereof and (ii) an internalizing moiety,

wherein the chimeric polypeptide has phosphoinositide phosphatase activity;

wherein said internalizing moiety is an antibody or antigen-binding fragment thereof,

wherein said antibody or antigen-binding fragment thereof is a monoclonal antibody 3E10, or a variant thereof that retains the cell penetrating activity of 3E10, or an antibody that binds the same epitope as 3E10, or an antigen-binding fragment of any of the foregoing.

2. The chimeric polypeptide of claim 1 , wherein the MTM1 polypeptide comprises an amino acid sequence having at least 90% sequence identity to SEQ ID NO: 1.

3. The chimeric polypeptide of claim 1 , wherein the MTM1 polypeptide further comprises one or more polypeptide portions that enhance one or more of in vivo stability, in vivo half life, uptake/administration, and/or purification.

4. The chimeric polypeptide of claim 1 , wherein the internalizing moiety promotes transport of said chimeric polypeptide into muscle cells.

5. The chimeric polypeptide of claim 4 , wherein said antibody or antigen-binding fragment thereof is chimeric or humanized.

6. The chimeric polypeptide of claim 4 , wherein said antibody or antigen-binding fragment thereof comprises a light chain comprising an amino acid sequence having at least 98% sequence identity to SEQ ID NO: 4 and a heavy chain comprising an amino acid sequence having at least 98% sequence identity to SEQ ID NO: 2.

7. The chimeric polypeptide of claim 1 , wherein the antibody or antigen-binding fragment comprises a heavy chain variable domain (VH) comprising the amino acid sequence set forth in SEQ ID NO: 2 and a light chain variable domain (VL) comprising the amino acid sequence set forth in SEQ ID NO: 4, or which is a humanized antibody or antigen-binding fragment thereof.

8. The chimeric polypeptide of claim 1 , wherein the internalizing moiety comprises a scFv.

9. The chimeric polypeptide of claim 1 , wherein the MTM1 polypeptide or bioactive fragment thereof is conjugated or joined to the internalizing moiety by a linker.

10. The chimeric polypeptide of claim 9 , wherein the internalizing moiety is conjugated to the N-terminal or C-terminal amino acid of the MTM1 polypeptide.

11. A composition comprising the chimeric polypeptide of claim 1 , and a pharmaceutically acceptable carrier.

12. The composition of claim 11 , further comprising a second agent which acts in an additive or synergistic manner for treating myotubular myopathy.

13. A nucleic acid construct, comprising a nucleotide sequence that encodes the chimeric polypeptide of claim 1 .

14. A nucleic acid construct, comprising a nucleotide sequence that encodes an MTM1 polypeptide or a bioactive fragment thereof, operably linked to a nucleotide sequence that encodes an internalizing moiety,

wherein the nucleic acid construct encodes a chimeric polypeptide having phosphoinositide phosphatase activity;

wherein said internalizing moiety is an antibody or antigen-binding fragment thereof,

wherein said antibody or antigen-binding fragment thereof is a monoclonal antibody 3E10, or a variant thereof that retains the cell penetrating activity of 3E10, or an antibody that binds the same epitope as 3E10, or an antigen-binding fragment of any of the foregoing.

15. The nucleic acid construct of claim 14 , wherein the antibody or antigen-binding fragment comprises a heavy chain variable domain (VH) comprising the amino acid sequence set forth in SEQ ID NO: 2 and a light chain variable domain (VL) comprising the amino acid sequence set forth in SEQ ID NO: 4, or which is a humanized antibody or antigen-binding fragment thereof.

16. The nucleic acid construct of claim 14 , wherein the internalizing moiety comprises a scFv.

17. A method of delivering a chimeric polypeptide into a muscle cell, comprising contacting a muscle cell with a chimeric polypeptide, which chimeric polypeptide comprises an MTM1 polypeptide or a bioactive fragment thereof and an internalizing moiety which promotes transport into muscle cells, thereby delivering the chimeric polypeptide into the muscle cell;

wherein said internalizing moiety is an antibody or antigen-binding fragment thereof,

wherein said antibody or antigen-binding fragment thereof is a monoclonal antibody 3E10, or a variant thereof that retains the cell penetrating activity of 3E10, or an antibody that binds the same epitope as 3E10, or an antigen-binding fragment of any of the foregoing.

18. The method of claim 17 , wherein the MTM1 polypeptide comprises an amino acid sequence having at least 90% sequence identity to SEQ ID NO: 1, or a bioactive fragment thereof.

19. The method of claim 17 , wherein the antibody or antigen-binding fragment comprises a heavy chain variable domain (VH) comprising the amino acid sequence set forth in SEQ ID NO: 2 and a light chain variable domain (VL) comprising the amino acid sequence set forth in SEQ ID NO: 4, or which is a humanized antibody or antigen-binding fragment thereof.

20. The method of claim 17 , wherein the internalizing moiety comprises a scFv.

Assignments (3)
MERGER Recorded Nov 8, 2013
From: VALERION THERAPEUTICS, INC.
To: VALERION THERAPEUTICS, LLC
Reel/Frame 031569/0225 →
CHANGE OF NAME Recorded Nov 8, 2013
From: 4S3 BIOSCIENCE, INC.
To: VALERION THERAPEUTICS, INC.
Reel/Frame 031609/0016 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 22, 2012
From: ARMSTRONG, DUSTIN D.
To: 4S3 BIOSCIENCE INC.
Reel/Frame 027740/0460 →
Continuity (2)
Provisional Application 61268732 · Jun 15, 2009
Related Publication 20120213760A1 · Aug 23, 2012