IP Library Granted Patent US 9,683,044
Granted Patent B2
US 9,683,044 · App. 13/971,584 · Granted Jun 20, 2017

Molecules with antigen binding and polyvalent FC gamma receptor binding activity

Inventors: David Block (Baltimore, MD); Henrik Olsen (Baltimore, MD)
Assignee: GLIKNIK INC.
C07K16/2863C07K16/241C07K16/2887C07K16/32A61K2039/505C07K2317/30C07K2317/52C07K2317/53C07K2317/55C07K2317/64C07K2317/73C07K2317/732
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Quick Facts
Patent No.
US 9,683,044
App. No.
13/971,584
Granted
Jun 20, 2017
Kind
B2
Abstract

The current invention involves biologically active proteins termed stradobodies. The stradobodies have two or more domains that create stradobody multimers. The stradobodies have both antigen-binding capacity and the ability to bind Fc receptors (FcR), and are useful in the treatment and prevention of disease.

Claims (18)

1. A stradobody comprising, from amino to carboxy terminus, an Fab domain, a first Fc domain, two multimerization domains independently selected from an isoleucine zipper and an IgG2 hinge, and a second Fc domain.

2. The stradobody of claim 1 , wherein the amino acid sequence of the IgG2 hinge domain is according to SEQ ID NO: 3, and wherein the IgG2 hinge is capable of multimerizing the stradobody.

3. The stradobody of claim 1 , wherein the amino acid sequence of the isoleucine zipper is according to SEQ ID NO: 32, and wherein the isoleucine zipper is capable of multimerizing the stradobody.

4. The stradobody of claim 1 , wherein at least one of the first and second Fc domains is an IgG1 Fc domain, wherein the IgG1 Fc domain comprises an IgG1 CH2 and IgG1 CH3.

5. The stradobody of claim 4 , wherein the IgG1 Fc domain further comprises an IgG1 hinge.

6. The stradobody of claim 1 , wherein the amino acid sequence of at least one IgG1 Fc domain is according to SEQ ID NO: 2.

7. The stradobody of claim 1 , wherein the stradobody comprises, from amino to carboxy terminus:

(a) an Fab domain;

(b) a first Fc domain;

(c) an isoleucine zipper;

(d) an IgG2 hinge; and

(e) a second Fc domain.

8. The stradobody of claim 7 , wherein said stradobody displays enhanced cellular toxicity compared to stradobodies containing one or more multimerization domains in locations other than separating two or more Fc domains.

9. The stradobody of claim 1 , wherein the Fab domain is specific for EGFR, Her2/neu or CD20.

10. The stradobody of claim 9 , wherein the amino acid sequence of the Fab domain is according to SEQ ID NO: 31, SEQ ID NO: 34 or SEQ ID NO: 36, wherein the Fab domain binds EGFR, Her2/neu, or CD20, respectively.

11. The stradobody of claim 1 , wherein the stradobody displays enhanced cell killing compared to a monoclonal antibody having the same antigen specificity.

12. The stradobody of claim 1 , wherein the stradobody displays enhanced inhibition of cellular proliferation compared to a monoclonal antibody having the same antigen specificity.

13. The stradobody of claim 1 wherein the amino acid sequence of the stradobody is SEQ ID NO: 35, 33, 37, or 66, wherein the stradobody binds Her2/neu, EGFR, CD20, or TNF, respectively.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 20, 2013
From: BLOCK, DAVID; OLSEN, HENRIK
To: GLIKNIK INC.
Reel/Frame 031642/0053 →
Continuity (3)
Provisional Application 61785144 · Mar 14, 2013
Provisional Application 61691057 · Aug 20, 2012
Related Publication 20140072582A1 · Mar 13, 2014