Carbohydrate content of CTLA4 molecules
The invention provides for mammalian cells capable of producing recombinant CTLA4-Ig and variants thereof. The invention also provides for compositions comprising CTLA4-Ig and formulations thereof. The invention further provides for methods for mass-producing CTLA4-Ig from mammalian cells capable of producing this recombinant protein, and for purifying the CTLA4-Ig.
1. A composition comprising cytotoxic T lymphocyte antigen 4-Ig (CTLA4-Ig) molecules, wherein the CTLA4-Ig composition comprises
(a) a N-acetyl neuraminic acid (NANA) molar ratio of from about 5.0 to about 10.0 mole of NANA/mole CTLA4-Ig molecule, and
(b) less than or equal to 5.0 area percent high molecular weight species as determined by size exclusion chromatography and spectrophotometric detection,
wherein the CTLA4-Ig molecules are isolated from a soluble fraction of a liquid culture medium comprising an initial population of CTLA4-Ig molecules recombinantly produced by mammalian cells, wherein
(1) the CTLA4-Ig molecules of the initial population have one or more sialic acid residues;
(2) the number of sialic acid residues per CTLA4-Ig molecule varies within the initial population;
(3) the initial population comprises CTLA4-Ig dimers and high molecular weight aggregates;
(4) the liquid culture medium contains Monocyte Chemotactic Protein-1 (MCP-1); and,
(5) the CTLA4-Ig molecules comprise one or more polypeptides having the amino acid sequence set forth in SEQ ID NO: 4, 11, 12, 13, 14, 15, or 16,
wherein the CTLA4-Ig composition is obtainable by a method comprising:
(i) obtaining the soluble fraction of the liquid culture medium, wherein the liquid culture medium comprises mammalian cells that produce the initial population of CTLA4-Ig molecules; then
(ii) subjecting the soluble fraction of the liquid culture medium to affinity chromatography to reduce MCP-1 content; then
(iii) subjecting the composition of step (ii) to anion chromatography to separate the CTLA4-Ig molecules into two or more fractions, wherein at least one fraction has a greater molar ratio of sialic acid to CTLA4-Ig molecules compared to at least one other fraction; and then
(iv) subjecting the composition of step (iii) to hydrophobic interaction chromatography to separate CTLA4-Ig dimers from CTLA4-Ig high molecular weight aggregates.
2. The CTLA4-Ig composition of claim 1 , wherein the mammalian cells are Chinese Hamster Ovary (CHO) cells.
3. The CTLA4-Ig composition of claim 1 , wherein the concentration of MCP-1 in the CTLA4-Ig composition after the method is less than about 5 ppm.
4. The CTLA4-Ig composition of claim 1 , wherein the CTLA4-Ig composition comprises a N-glycolyl neuraminic acid (NGNA) molar ratio of less than 1.5 mole NGNA/mole CTLA4-Ig molecule.
5. The CTLA4-Ig composition of claim 1 , wherein the CTLA4-Ig composition comprises mannose from about 10 to about 20 moles/mole CTLA4-Ig molecule.
6. The CTLA4-Ig composition of claim 1 , wherein the CTLA4-Ig composition comprises fucose from about 4.2 to about 7.0 moles/mole CTLA4-Ig molecule.
7. The CTLA4-Ig composition of claim 1 , wherein the CTLA4-Ig composition comprises galactose from about 9.2 to about 17 moles/mole CTLA4-Ig molecule.
8. The CTLA4-Ig composition of claim 1 , wherein the CTLA4-Ig composition comprises mannose from about 10 to about 20 moles/mole CTLA4-Ig molecule, fucose from about 4.2 to about 7.0 moles/mole CTLA4-Ig molecule, and galactose from about 9.2 to about 17 moles/mole CTLA4-Ig molecule.
9. The CTLA4-Ig composition of claim 4 , wherein the CTLA4-Ig composition comprises mannose from about 10 to about 20 moles/mole CTLA4-Ig molecule, fucose from about 4.2 to about 7.0 moles/mole CTLA4-Ig molecule, and galactose from about 9.2 to about 17 moles/mole CTLA4-Ig molecule.
10. The CTLA4-Ig composition of claim 9 , wherein the mammalian cells are CHO cells.
11. The CTLA4-Ig composition of claim 10 , wherein the CHO cells are a clonal population of CHO cells.
12. The CTLA4-Ig composition of claim 1 , wherein the CTLA4-Ig composition comprises a polypeptide having the amino acid sequence set forth in SEQ ID NO: 16.
13. The CTLA4-Ig composition of claim 12 , wherein the mammalian cells are CHO cells.
14. The CTLA4-Ig composition of claim 12 , wherein the concentration of MCP-1 in the CTLA4-Ig composition after the method is less than about 5 ppm.
15. The CTLA4-Ig composition of claim 12 , wherein the CTLA4-Ig composition comprises a NGNA molar ratio of less than 1.5 mole NGNA/mole CTLA4-Ig molecule.
16. The CTLA4-Ig composition of claim 12 , wherein the CTLA4-Ig composition comprises mannose from about 10 to about 20 moles/mole CTLA4-Ig molecule.
17. The CTLA4-Ig composition of claim 12 , wherein the CTLA4-Ig composition comprises fucose from about 4.2 to about 7.0 moles/mole CTLA4-Ig molecule.
18. The CTLA4-Ig composition of claim 12 , wherein the CTLA4-Ig composition comprises galactose from about 9.2 to about 17 moles/mole CTLA4-Ig molecule.
19. The CTLA4-Ig composition of claim 12 , wherein the CTLA4-Ig composition comprises mannose from about 10 to about 20 moles/mole CTLA4-Ig molecule, fucose from about 4.2 to about 7.0 moles/mole CTLA4-Ig molecule, and galactose from about 9.2 to about 17 moles/mole CTLA4-Ig molecule.
20. The CTLA4-Ig composition of claim 15 , wherein the CTLA4-Ig composition comprises mannose from about 10 to about 20 moles/mole CTLA4-Ig molecule, fucose from about 4.2 to about 7.0 moles/mole CTLA4-Ig molecule, and galactose from about 9.2 to about 17 moles/mole CTLA4-Ig molecule.
21. The CTLA4-Ig composition of claim 20 , wherein the mammalian cells are CHO cells.
22. The CTLA4-Ig composition of claim 21 , wherein the CHO cells are a clonal population of CHO cells.