PRODUCTION OF PROTEINS
The present invention is of a method of producing proteins in mammalian cells using a permanent selection in the absence of cytotoxic drugs. Specifically, the present invention can be used to produce large quantities of highly pure human proteins which are suitable for pharmaceutical applications.
1 . A method of selecting for positively-transformed cells comprising:
(a) providing eukaryotic cells lacking activity of an endogenous cell viability protein;
(b) transforming said eukaryotic cells with a nucleic acid construct encoding said cell viability protein or at least a functional portion thereof; and
(c) culturing said eukaryotic cells transformed with said nucleic acid construct under conditions such that cell viability is dependent upon normal activity of said cell viability protein thereby selecting for positively-transformed cells.
2 . The method of claim 1 , wherein said nucleic acid construct further encodes a protein-of-interest.
3 . The method of claim 1 , wherein said cell viability protein is selected from the group consisting of galaktokinase 1, reduced folate carrier, thymidine kinase, adenosine kinase, tryptophan synthase, histidinol dehydrogenase and glutamine synthetase.
4 . The method of claim 1 , wherein said eukaryotic cells are selected from the group consisting of yeast cells, insect cells, plant cells and mammalian cells.
5 . The method of claim 2 , wherein said protein-of-interest is selected from the group consisting of a growth factor, an hormone, a cytokine, an extracellular protein, a cell adhesion protein, and a cell signaling protein.
6 . The method of claim 5 , wherein said protein-of-interest is selected from the group consisting of epidermal growth factor, transforming growth factor-beta, fibroblast growth factor-acidic, fibroblast growth factor-basic, erythropoietin, thrombopoietin, hepatocyte growth factor, insulin-like growth factor-I, insulin-like growth factor-Il, interferon-gamma, platelet-derived growth factor, prolactin, parathyroid hormone, gastrin, leptin, growth hormone, insulin and CG-β, SDF-1α, IL-7, IL-10, IL-20, IL-19, fibrinogen, collagen, fibronectin, vimentin, microtubule-associated protein 1b, neurite outgrowth factor (NOF), bacterial cellulose (BC), laminin, integrin, intercellular adhesion molecule (ICAM) 1, N-CAM, cadherin, tenascin, gicerin, nerve injury induced protein 2 (ninjurin2), p38 mitogen-activated protein kinase, nuclear factor 20 kappaB, Raf kinase inhibitor protein (RKIP), Raf-1, MEK, protein kinase C (PKC), phosphoinositide-3-kinase gamma, receptor tyrosine kinases, heterotrimeric G-proteins, Caveolin-3, and 14-3-3 proteins.
7 - 11 . (canceled)
12 . The method of claim 1 , wherein said nucleic acid construct includes a nucleic acid sequence as set forth in SEQ ID NO:3.
13 . The method of claim 1 , wherein said nucleic acid construct includes a nucleic sequence as set forth in SEQ ID NO:4.
14 . The method of claim 3 , wherein said cell viability protein is Galactokinase 1 and whereas said culturing is effected in the presence of D-Galactose.
15 . The method of claim 3 , wherein said cell viability protein is reduced folate carrier and whereas said culturing is effected in the presence of a reduced folate.
16 . The method of claim 15 , wherein said reduced folate is leucovorin.
17 . The method of claim 14 , wherein a concentration of said D-Galactose is selected from a range of 0.01-10 mM.
18 . The method of claim 14 , wherein a concentration of said D-Galactose is 0.25 mM.
19 . The method of claim 16 , wherein a concentration of said leucovorin is selected from a range of 0.01-5 nM.
20 . The method of claim 16 , wherein a concentration of said leucovorin is 0.25 nM.
21 . A cytotoxic-free eukaryotic cell culture comprising cells genetically modified to express a cell viability protein and a protein-of-interest under culturing conditions such that cell viability is dependent upon normal activity of said cell viability protein.
22 . The cell culture of claim 21 , wherein said cell viability protein is selected from the group consisting of galaktokinase 1, reduced folate carrier, thymidine kinase, adenosine kinase, tryptophan synthase, histidinol dehydrogenase and glutamine synthetase.
23 . The cell culture of claim 21 , wherein said cells are selected from the group consisting of yeast cells, insect cells, plant cells and mammalian cells.
24 . The cell culture of claim 21 , wherein said protein-of-interest is selected from the group consisting of a growth factor, an hormone, a cytokine, an extracellular protein, a cell adhesion protein, and a cell signaling protein.
25 . The cell culture of claim 24 , wherein said protein-of-interest is selected from the group consisting of epidermal growth factor, transforming growth factor-beta, fibroblast growth factor-acidic, fibroblast growth factor-basic, erythropoietin, thrombopoietin, hepatocyte growth factor, insulin-like growth factor-I, insulin-like growth factor-II, interferon-gamma, platelet-derived growth factor, prolactin, parathyroid hormone, gastrin, leptin, growth hormone, insulin, CG-β, SDF-1α, IL-7, IL-10, IL-20, IL-19, fibrinogen, collagen, fibronectin, vimentin, microtubule-associated protein 1b, neurite outgrowth factor (NOF), bacterial cellulose (BC), laminin, integrin, intercellular adhesion molecule (ICAM) 1, N-CAM, cadherin, tenascin, gicerin, nerve injury induced protein 2 (ninjurin2), p38 mitogen-activated protein kinase, nuclear factor 20 kappaB, Raf kinase inhibitor protein (RKIP), Raf-1, MEK, protein kinase C (PKC), phosphoinositide-3-kinase gamma, receptor tyrosine kinases, heterotrimeric G-proteins, caveolin-3, and 14-3-3 proteins.
26 - 30 . (canceled)
31 . The cell culture of claim 22 , wherein said cell viability protein is Galactokinase 1 and whereas said culturing conditions include D-Galactose.
32 . The cell culture of claim 22 , wherein said cell viability protein is reduced folate carrier and whereas said culturing conditions include a reduced folate.
33 . The cell culture of claim 32 , wherein said reduced folate is leucovorin.
34 . The cell culture of claim 31 , wherein a concentration of said DGalactose is selected from a range of 0.01-10 mM.
35 . The cell culture of claim 31 , wherein a concentration of said DGalactose is 0.25 mM.
36 . The cell culture of claim 33 , wherein a concentration of said leucovorin is selected from a range of 0.01-10 nM.
37 . The cell culture of claim 33 , wherein a concentration of said 20 leucovorin is 0.25 nM.
38 . A method of producing a protein-of-interest, comprising:
(a) transforming eukaryotic cells lacking activity of an endogenous cell viability protein with a nucleic acid construct encoding the protein-of-interest and said cell viability protein or at least a functional portion thereof;
(b) culturing said eukaryotic cells transformed with said nucleic acid construct under conditions such that cell viability is dependent upon normal activity of said cell viability protein thereby selecting for positively-transformed eukaryotic cells; and
(c) purifying the protein-of-interest from said positively-transformed eukaryotic cells or a culture medium thereof.
39 . The method of claim 38 , wherein said cell viability protein is selected from the group consisting of galaktokinase 1, reduced folate carrier, thymidine kinase, adenosine kinase, tryptophan synthase, histidinol dehydrogenase and glutamine synthetase.
40 . The method of claim 38 , wherein said eukaryotic cells are selected from the group consisting of yeast cells, insect cells, plant cells and mammalian cells.
41 . The method of claim 38 , wherein said protein-of-interest is selected from the group consisting of a growth factor, an hormone, a cytokine, an extracellular protein, a cell adhesion protein, and a cell signaling protein.
42 . The method of claim 41 , wherein said protein-of-interest is selected from the group consisting of epidermal growth factor, transforming growth factor-beta, fibroblast growth factor-acidic, fibroblast growth factor-basic, erythropoietin, thrombopoietin, hepatocyte growth factor, insulin-like growth factor-I, insulin-like growth factor-II, interferon gamma, platelet-derived growth factor, prolactin, parathyroid hormone, gastrin, leptin, growth hormone, insulin, CG-β, SDF-1α, IL-7, IL-10, IL-20, IL-19, fibrinogen, collagen, fibronectin, vimentin, microtubule-associated protein 1b, neurite outgrowth factor (NOF), bacterial cellulose (BC), laminin, integrin, intercellular adhesion molecule (ICAM) 1, N-CAM, cadherin, tenascin, gicerin, nerve injury induced protein 2 (ninjurin2), p38 mitogen-activated protein kinase, nuclear factor 20 kappaB, Raf kinase inhibitor protein (RKIP), Raf-1, MEK, protein kinase C (PKC), phosphoinositide-3-kinase gamma, receptor tyrosine kinases, heterotrimeric G-proteins, caveolin-3, and 14-3-3 proteins.
43 - 47 . (canceled)
48 . The method of claim 38 , wherein said nucleic acid construct includes a nucleic acid sequence as set forth in SEQ ID NO:3.
49 . The method of claim 38 , wherein said nucleic acid construct includes a nucleic sequence as set forth in SEQ ID NO:4.
50 . The method of claim 38 , wherein said cell viability protein is Galactokinase 1 and whereas said culturing is effected in the presence of D-Galactose.
51 . The method of claim 38 , wherein said cell viability protein is reduced folate carrier and whereas said culturing is effected in the presence of a reduced folate.
52 . The method of claim 51 , wherein said reduced folate is leucovorin.
53 . The method of claim 50 , wherein a concentration of said D-Galactose is selected from a range of 0.01-10 mM.
54 . The method of claim 50 , wherein a concentration of said D-Galactose is 0.25 mM.
55 . The method of claim 52 , wherein a concentration of said leucovorin is selected from a range of 0.01-10 nM.
56 . The method of claim 52 , wherein a concentration of said leucovorin is 0.25 nM.