Inducible eukaryotic expression system
Compositions and methods for the inducible expression of genes in eukaryotic cells are provided. Expression of a nucleotide sequence of interest encoding a protein of interest is controlled by a regulatory fusion protein that consists of a transcription blocking domain and a ligand-binding domain. When a cognate ligand for the ligand-binding domain is present, transcription of the nucleotide sequence of interest is blocked. Upon removal of the cognate ligand, the nucleotide sequence of interest is transcribed. The method is useful for large scale bioreactor production of a desired protein of interest in eukaryotic cells.
1. A method for expressing a protein of interest from a gene of interest in eukaryotic cells in a bioreactor, comprising:
(a) seeding a starter culture for a bioreactor with eukaryotic cells in the presence of a concentration of a ligand that stabilizes a regulatory fusion protein (RFP) and inhibits expression of a protein of interest, wherein the eukaryotic cells comprise
i. a promoter operably linked to the gene of interest encoding the protein of interest and controlled by a Tet or Arc operator operably linked and positioned 5′ with respect to the promoter, and,
ii. a gene encoding the regulatory fusion protein (RFP), wherein the RFP consists essentially of
(1) a transcription blocking domain comprising (i) a TetR repressor or (ii) an Arc repressor DNA-binding domain; and
(2) a ligand-binding domain of an estrogen receptor of SEQ ID NO:8,
wherein the RFP inhibits expression of the gene of interest by binding to the Tet or Arc operator and inhibiting transcription in the presence of the ligand, but not in the absence of the ligand;
wherein the ligand is capable of binding to the ligand-binding domain of an estrogen receptor;
(b) growing the cells in the starter culture to establish a culture, wherein expression of the protein of interest is inhibited;
(c) seeding a 10 liter bioreactor with the culture, wherein media employed in the 10 liter bioreactor comprises an inhibitory amount of the ligand;
(d) conducting a seed train to seed a 3,000 liter or 10,000 liter bioreactor, wherein media added subsequent to the 10 liter bioreactor does not contain the ligand, and wherein the seed train is conducted so that sufficient media is added to reduce the concentration of the ligand at the 3,000 liter or 10,000 liter stage; and
(e) growing the cells of the 3,000 liter or 10,000 liter bioreactor under conditions sufficient to express the protein of interest.
2. The method according to claim 1 , wherein the protein of interest is an antibody.
3. The method according to claim 1 , wherein the estrogen receptor ligand-binding domain comprises the amino acid sequence from N304 to V595 of SEQ ID NO:8.
4. The method according to claim 1 , wherein the estrogen receptor ligand-binding domain has amino acid modifications valine at residue 400, alanine at residue 543, and alanine at residue 544 of the estrogen receptor (SEQ ID NO:8).
5. The method according to claim 1 , wherein the ligand is selected from the group consisting of estrogen, tamoxifen, and 4-hydroxytamoxifen (OHT).
6. The method according to claim 1 , wherein the TetR repressor comprises amino acids M1 to S207 of SEQ ID NO:7.
7. The method according to claim 1 , wherein the Arc repressor is an Arc repressor dimer.
8. The method according to claim 7 , wherein the Arc repressor dimer comprises Arc monomers connected by a linker.
9. The method of claim 1 , wherein the promoter operably linked to the nucleotide sequence of interest is derived from CMV, SV40, Rous sarcoma virus, metallothionein, nopaline synthetase, cauliflower mosaic virus 35S RNA, ribulose biphosphate carboxylase, Gal4, alcohol dehydrogenase, phosphoglycerol kinase, alkaline phosphatase, elastase I, insulin, immunoglobulin, mouse mammary tumor virus, albumin, α-fetoprotein, α1-antitrypsin, β-globin, or myosin light chain-2.
10. The method of claim 9 , wherein the promoter is CMV-MIE.
11. The method of claim 1 , wherein the eukaryotic cell is selected from the group consisting of a COS, CHO, 293, BHK or NSO cell.
12. The method of claim 1 , wherein the operator is TetO or ArcO.
13. The method of claim 1 , wherein the operator is placed immediately downstream of the promoter.
14. The method of claim 1 , wherein the operator is placed within 10 base pairs of the promoter.
15. The method according to claim 1 , wherein the bioreactor has a capacity of 10 liters to 10,000 liters.
16. The method according to claim 15 , wherein the bioreactor has a capacity of 10 liters to 3,000 liters.
17. The method according to claim 1 , wherein the cells are grown in a seed train for a bioreactor, wherein the seed train comprises a 10 liter stage, a 50 liter stage, a 500 liter stage, a 3,000 liter stage, and a 10,000 liter stage, and the concentration of ligand is reduced at each stage following the 10 liter stage, such that the reduced concentration of ligand at the 10,000 liter stage is sufficient to express the protein of interest.
18. The method according to claim 17 , wherein the concentration of ligand is reduced at each stage following the 10 liter stage, such that the reduced concentration of ligand at the 3,000 liter stage is sufficient to express the protein of interest.
19. The method of claim 17 , wherein the concentration of ligand is reduced by adding media that does not contain any ligand that binds to the ligand-binding domain of an estrogen receptor.
20. The method of claim 17 , wherein the concentration of ligand is reduced by media exchange for media that does not contain any ligand that binds to the ligand-binding domain of an estrogen receptor.