IP Library Granted Patent US 11,535,673
Granted Patent B2
US 11,535,673 · App. 12/594,747 · Granted Dec 27, 2022

Chimeric activators: quantitatively designed protein therapeutics and uses thereof

Inventors: Pamela A. Silver (Cambridge, MA); Pablo Gabriel Cironi Lopez (Madrid, ES); David G. Miguez (Barcelona, ES)
Assignee: President and Fellows of Harvard CoHege
C07K16/2863A61K47/642A61K47/6425A61K47/6813A61K47/6849A61K47/6853C07K14/485C07K14/525C07K14/56C07K14/5759C07K16/2896C07K16/3007A61K38/00C07K2317/34C07K2317/622C07K2317/76C07K2319/30C07K2319/33C07K2319/74
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Quick Facts
Patent No.
US 11,535,673
App. No.
12/594,747
Granted
Dec 27, 2022
Kind
B2
Abstract

Aspects of the invention provide methods for harnessing the potential of proteins that occur naturally (e.g., in humans) and that have serious but finite toxicity. Aspects of the invention relate to a quantitative systems-biological and structural approach to design a class Mof chimeric proteins that avoid the toxicity of protein drugs while retaining their desired activities. In particular, chimeric proteins containing a variant form of a natural protein fused to a targeting moiety may be administered to a subject to target a signal (e.g., induction of apoptosis) to particular cells without having a generalized toxic effect.

Claims (12)

1. A recombinant protein comprising

a first element comprising a variant of interferon alpha (IFNa) comprising at least one amino acid substitution mutation that reduces the binding affinity of the variant by at least 10-fold relative to IFNα, and wherein the variant of IFNa is a K133A, R144A, or R149A variant of IFNα;

a second element comprising Epidermal Growth Factor (EGF), Cell Differentiation 4 (CD4), or an anti-EGFRde(2-7); and

a linker that connects the first and second elements.

2. The recombinant protein of claim 1 , wherein the linker is 35 amino acids long.

3. The recombinant protein of claim 1 , wherein the linker consists of glycine and serine residues.

4. The recombinant protein of claim 1 , wherein the variant of IFNα comprises at least one amino acid substitution mutation that reduces the binding affinity of the variant of IFNα for its naturally-occurring cell surface receptors by at least 200-fold relative to the wild-type of IFNα protein.

5. The recombinant protein of claim 1 , wherein the second element comprises an EGF protein.

6. The recombinant protein of claim 1 , wherein the variant of IFNα comprises a R144A mutation or a R149A mutation; and the second element comprises an EGF protein.

7. The recombinant protein of claim 1 , wherein the recombinant protein binds to a cancer cell and mediates cell death or a reduction or absence of cell proliferation of the cancer cell; and the variant of IFNα alone will not bind to the cancer cell and mediate cell death or a reduction or absence of cell proliferation of the cancer cell.

8. The recombinant protein of claim 1 , wherein the linker is between 25 and 70 amino acids long.

9. The recombinant protein of claim 1 , wherein the linker is flexible.

Assignments (2)
CORRECTIVE ASSIGNMENT TO CORRECT THE SECOND INVENTOR'S NAME PREVIOUSLY RECORDED AT REEL: 24219 FRAME: 377. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Apr 2, 2019
From: SILVER, PAMELA A.; CIRONI LOPEZ, PABLO GABRIEL; MIGUEZ, DAVID G.
To: PRESIDENT AND FELLOWS OF HARVARD COLLEGE
Reel/Frame 048765/0085 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 12, 2010
From: MIGUEZ, DAVID G.; SILVER, PAMELA A.; CIRONI, PABLO
To: PRESIDENT AND FELLOWS OF HARVARD COLLEGE
Reel/Frame 024219/0377 →
Continuity (4)
Provisional Application 60910390 · Apr 5, 2007
Provisional Application 61005775 · Dec 7, 2007
Provisional Application 61065937 · Feb 15, 2008
Related Publication 20110274658A1 · Nov 10, 2011
Cited By (1)
US 12,275,796