IP Library Granted Patent US 8,455,205
Granted Patent B2
US 8,455,205 · App. 13/191,411 · Granted Jun 4, 2013

Metalloproteinase 9 binding proteins

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Quick Facts
Patent No.
US 8,455,205
App. No.
13/191,411
Granted
Jun 4, 2013
Kind
B2
Abstract

Proteins that bind to matrix metalloproteinase 9 and methods of using such proteins are described.

Claims (19)

1. A method of inhibiting an interaction between Matrix Metalloproteinase-9 (MMP-9) and an MMP-9 substrate, the method comprising: contacting an MMP-9 binding protein with MMP-9 in the presence of an MMP-9 substrate,

wherein the MMP-9 binding protein comprises at least one immunoglobulin variable region,

wherein the MMP-9 binding protein comprises heavy chain variable domain comprising a HC-CDR1 comprising the amino acid sequence of SEQ ID NO: 956, a HC-CDR2 comprising the amino acid sequence of SEQ ID NO: 957, a HC-CDR3 comprising the amino acid sequence of SEQ ID NO: 958, and a light chain variable region comprising an LC-CDR1 comprising the amino acid sequence of SEQ ID NO: 953, a LC-CDR2 comprising the amino acid sequence of SEQ ID NO: 954, and a LC-CDR3 region comprising the amino acid sequence of SEQ ID NO: 955, and

wherein the binding protein binds to MMP-9 and thereby inhibits the binding of the MMP-9 substrate to MMP-9.

2. The method of claim 1 , wherein the MMP-9 binding protein comprises a heavy chain variable domain that is at least 85% identical to SEQ ID NO: 934.

3. The method of claim 1 , wherein the MMP-9 binding protein comprises a light chain variable domain that is at least 85% identical to SEQ ID NO: 933.

4. The method of claim 1 , wherein the MMP-9 binding protein is a Fab fragment or a full-length IgG.

5. The method of claim 1 , wherein the contacting step is performed in vitro or in vivo.

6. The method of claim 1 , wherein the MMP-9 binding protein is conjugated to a drug.

7. The method of claim 6 , wherein the drug is a cytotoxic or cytostatic agent.

8. The method of claim 1 , wherein the MMP-9 binding protein is a human or humanized antibody.

9. The method of claim 1 , wherein the MMP-9 binding protein binds to MMP-9 with a K D of less than 100 nM.

10. The method of claim 1 , wherein the MMP-9 binding protein binds to MMP-9 with a K D of less than 10 nM.

11. The method of claim 1 , wherein the MMP-9 binding protein binds to MMP-9 with a K D of less than 1 nM.

12. The method of claim 1 , wherein the MMP-9 binding protein inhibits MMP-9.

13. The method of claim 1 , wherein the MMP-9 binding protein has an IC50 of less than 100 nM.

14. The method of claim 1 , wherein the MMP-9 binding protein has an IC50 of less than 10 nM.

15. The method of claim 1 , wherein the MMP-9 binding protein has an IC50 of less than 1 nM.

16. The method of claim 7 , wherein the cytotoxic agent is selected from the group consisting of an auristatin, a DNA minor groove binding agent, a DNA minor groove alkylating agent, an enediyne, a lexitropsin, a duocarmycin, a taxane, a puromycin, a dolastatin, a podophyllotoxin, a baccatin derivative, a cryptophysin, a combretastatin, a maytansinoid, a vinca alkaloid, and an antitubulin agent.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 18, 2021
From: DYAX CORP.
To: TAKEDA PHARMACEUTICAL COMPANY LIMITED
Reel/Frame 056268/0983 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 2, 2018
From: DEVY, LAETITIA; BUCKLER, DAVID; COHEN, EDWARD H.
To: DYAX CORP.
Reel/Frame 046254/0647 →