IP Library Granted Patent US 8,815,238
Granted Patent B2
US 8,815,238 · App. 13/956,499 · Granted Aug 26, 2014

Methods for Preparing TACI-immunoglobulin fusion proteins

Inventors: Mark W. Rixon (Issaquah, WA); Jane A. Gross (Seattle, WA)
Assignee: ZymoGenetics, Inc.
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Quick Facts
Patent No.
US 8,815,238
App. No.
13/956,499
Granted
Aug 26, 2014
Kind
B2
Abstract

Molecules that interfere with the binding of a tumor necrosis factor receptor with its ligand, such as a soluble receptor, have proven usefulness in both basic research and as therapeutics. The present invention provides improved soluble transmembrane activator and calcium modulator and cyclophilin ligand-interactor (TACI) receptors.

Claims (18)

1. A mammalian host cell comprising a nucleic acid molecule construct encoding a fusion protein comprising

(a) a first polynucleotide encoding a transmembrane activator and calcium modulator and cyclophilin ligand-interactor (TACI) receptor moiety, wherein the TACI receptor moiety consists of amino acid residue 30 to 154 of SEQ ID NO:2 and wherein the TACI receptor moiety binds at least one of ZTNF2 or ZTNF4; and,

(b) a second polynucleotide encoding an immunoglobulin moiety that comprises a C H2 and a C H3 domain;

wherein said first and said second polynucleotide encode said fusion protein.

2. The mammalian host cell of claim 1 , wherein said nucleic acid molecule construct is operably linked to a promoter that directs transcription of the encoded fusion protein.

3. The mammalian host cell of claim 1 , wherein said nucleic acid molecule construct of claim 1 , further comprises a third polynucleotide encoding a secretory sequence.

4. The mammalian host cell of claim 1 , wherein the immunoglobulin moiety is an IgG1 Fc fragment that comprises a disulfide linked heavy chain hinge region, a C H2 domain and a C H3 domain.

5. The mammalian host cell of claim 1 , wherein the fusion protein has an amino acid sequence comprising the secreted form of the amino acid sequence of SEQ ID NO:54.

6. The mammalian host cell of claim 1 , wherein the fusion protein comprises the amino acid sequence of SEQ ID NO:54, wherein the optimized tPA (otPA) leader sequence (SEQ ID NO:25) has been removed.

7. A method of expressing a fusion protein comprising culturing a mammalian host cell under conditions that allow for the expression of a fusion protein wherein said fusion protein is encoded by a nucleic acid molecule construct comprising

(a) a first polynucleotide encoding a transmembrane activator and calcium modulator and cyclophilin ligand-interactor (TACI) receptor moiety, wherein the TACI receptor moiety consists of amino acid residue 30 to 154 of SEQ ID NO:2 and wherein the TACI receptor moiety binds at least one of ZTNF2 or ZTNF4; and,

(b) a second polynucleotide encoding an immunoglobulin moiety that comprises a C H2 and a C H3 domain;

wherein said first and said second polynucleotide encode said fusion protein.

8. The method of claim 7 further comprising isolating said fusion protein.

9. The method of claim 7 , wherein said nucleic acid molecule construct, further comprises a third polynucleotide encoding a secretory sequence.

10. The method of claim 9 , wherein the immunoglobulin moiety is an IgG1 Fc fragment that comprises a disulfide linked heavy chain hinge region, a C H2 domain and a C H3 domain.

11. The method of claim 7 , wherein the fusion protein has an amino acid sequence comprising the secreted form of the amino acid sequence of SEQ ID NO:54.

12. The method of claim 7 , wherein the fusion protein comprises the amino acid sequence of SEQ ID NO:54, wherein the optimized tPA (otPA) leader sequence (SEQ ID NO:25) has been removed.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 26, 2021
From: RIXON, MARK W.; GROSS, JANE A.
To: ZYMOGENETICS, INC.
Reel/Frame 056044/0246 →
Continuity (7)
Continuation 13105182 · May 11, 2011
Division 12605561 · Oct 26, 2009
Continuation 12359801 · Jan 26, 2009
Division 11242294 · Oct 3, 2005
Continuation 10152363 · May 20, 2002
Provisional Application 60293343 · May 24, 2001
Related Publication 20130309231A1 · Nov 21, 2013