IP Library Granted Patent US 9,309,311
Granted Patent B2
US 9,309,311 · App. 13/801,189 · Granted Apr 12, 2016

Method for making Heteromultimeric molecules

Inventors: Austin L. Gurney (San Francisco, CA); Aaron K. Sato (Burlingame, CA)
Assignee: OncoMed Pharmaceuticals, Inc.
C07K16/22C07K16/18C07K16/468A61K47/48546C07K2316/96C07K2317/20C07K2317/31C07K2317/52C07K2317/526C07K2317/55C07K2317/565C07K2317/73C07K2317/76C12N15/00
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Quick Facts
Patent No.
US 9,309,311
App. No.
13/801,189
Granted
Apr 12, 2016
Kind
B2
Abstract

Methods for making heteromultimeric molecules, such as bispecific antibodies, and compositions comprising these molecules are disclosed. The methods include introducing mutations in amino acids that are in contact at the interface of two polypeptides, such that the electrostatic interaction between the ion pairs is altered.

Claims (13)

1. A method of preparing a bispecific antibody that specifically binds VEGF and DLL4, wherein the bispecific antibody comprises a first and a second human immunoglobulin heavy chain polypeptide and a first and a second immunoglobulin light chain polypeptide, wherein the first and second immunoglobulin heavy chain polypeptide each comprise a CH3 domain and the CH3 domains comprise substitutions that promote heterodimerization of the first and second immunoglobulin heavy chain polypeptides, and wherein the first and second light chain polypeptides are identical in amino acid sequence, the method comprising substituting amino acids residues within the immunoglobulin heavy chain CH3 domains, and wherein the bispecific antibody is selected from the group consisting of:

(a) a human IgG1, wherein the substitutions consist of: a glutamate or aspartate at positions in the first immunoglobulin heavy chain polypeptide corresponding to positions 253 and 292 of SEQ ID NO:33, and a lysine at positions in the second immunoglobulin heavy chain polypeptide corresponding to positions 240 and 282 of SEQ ID NO:33;

(b) a human IgG2, wherein the substitutions consist of: a glutamate or aspartate at positions in the first immunoglobulin heavy chain polypeptide corresponding to positions 249 and 288 of SEQ ID NO:34 and a lysine at positions in the second immunoglobulin heavy chain polypeptide corresponding to positions 236 and 278 of SEQ ID NO:34;

(c) a human IgG3, wherein the substitutions consist of: a glutamate or aspartate at positions in the first immunoglobulin heavy chain polypeptide corresponding to positions 300 and 339 of SEQ ID NO:35, and a lysine at positions in the second immunoglobulin heavy chain polypeptide corresponding to positions 287 and 329 of SEQ ID NO:35; and

(d) a human IgG4, wherein the substitutions consist of: a glutamate or aspartate at positions in the first immunoglobulin heavy chain polypeptide corresponding to positions 250 and 289 of SEQ ID NO:36, and a lysine at positions in the second immunoglobulin heavy chain polypeptide corresponding to positions 237 and 279 of SEQ ID NO:36.

2. The method of claim 1 , wherein the bispecific antibody is a human IgG2 antibody and the CH3 domain of the first immunoglobulin heavy chain polypeptide comprises SEQ ID NO:5 or SEQ ID NO:7, and the CH3 domain of the second immunoglobulin heavy chain polypeptide comprises SEQ ID NO:9.

3. The method of claim 1 , wherein the bispecific antibody is a human IgG2 antibody, and wherein the substitutions consist of: a glutamate or aspartate at positions in the first immunoglobulin heavy chain polypeptide corresponding to positions 249 and 288 of SEQ ID NO:34, and a lysine at positions in the second immunoglobulin heavy chain polypeptide corresponding to positions 236 and 278 of SEQ ID NO:34.

4. The method of claim 1 , wherein the bispecific antibody comprises a VEGF binding sequence, wherein the VEGF binding sequence comprises a heavy chain variable region of SEQ ID NO:10 and a light chain variable region of SEQ ID NO:31 or SEQ ID NO:32.

5. The method of claim 4 , wherein the VEGF binding sequence comprises a heavy chain of SEQ ID NO:11 and a light chain of SEQ ID NO:13 or SEQ ID NO:15.

6. The method of claim 4 , wherein the bispecific antibody comprises a DLL4 binding sequence, wherein the DLL4 binding sequence has the same specificity as the 21M18 antibody produced by the hybridoma with ATCC designation PTA-8670.

7. The method of claim 1 , wherein the bispecific antibody further comprises a cytotoxin or a radioisotope.

8. The method of claim 1 , wherein each immunoglobulin heavy chain polypeptide is linked to the immunoglobulin light chain polypeptide.

9. The method of claim 1 , wherein the bispecific antibody comprises a DLL4 binding sequence that has the same specificity as the 21M18 antibody produced by the hybridoma with ATCC designation PTA-8670.

Assignments (5)
RELEASE OF SECURITY INTEREST Recorded Dec 15, 2020
From: KREOS CAPITAL V (UK) LIMITED
To: MEREO BIOPHARMA 5, INC.
Reel/Frame 054650/0289 →
CHANGE OF NAME Recorded Oct 5, 2020
From: ONCOMED PHARMACEUTICALS, INC.
To: MEREO BIOPHARMA 5, INC.
Reel/Frame 053981/0430 →
RELEASE OF SECURITY INTEREST Recorded Jan 13, 2020
From: KREOS CAPITAL V (UK) LIMITED
To: ONCOMED PHARMACEUTICALS, INC.
Reel/Frame 051574/0498 →
SECURITY INTEREST Recorded Jul 19, 2019
From: ONCOMED PHARMACEUTICALS, INC.
To: KREOS CAPITAL V (UK) LIMITED
Reel/Frame 049807/0948 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 11, 2013
From: GURNEY, AUSTIN L.; SATO, AARON K.
To: ONCOMED PHARMACEUTICALS, INC.
Reel/Frame 030586/0031 →
Continuity (4)
Division 12768650 · Apr 27, 2010
Provisional Application 61173129 · Apr 27, 2009
Provisional Application 61177412 · May 12, 2009
Related Publication 20130253172A1 · Sep 26, 2013