Purification process for removal of tyrosine sulfation antibody variants; purified compositions
The present invention relates to purified antibody and antigen-binding fragment compositions that lack sulfated tyrosine on one or more tyrosine residues in the immunoglobulin chains. Purification methods for removing sulfated tyrosine variants from antibody and antigen-binding fragment compositions are also provided.
1. A purified composition comprising non-CDR-L1 tyrosine sulfated antibodies that specifically bind to human lymphocyte activation gene 3 (anti-hLAG3) comprising: a heavy chain amino acid sequence of SEQ ID NO: 52 and a light chain amino acid sequence of SEQ ID NO: 51, and less than about 0.5% CDR-L1 tyrosine sulfated anti-hLAG3antibodies as compared to non-CDR-L1 tyrosine sulfated anti-hLAG3 antibodies as determined by mass spectrometry, wherein the CDR-L1 tyrosine sulfated anti-hLAG3 antibodies comprise a heavy chain amino acid sequence of SEQ ID NO: 52 and a light chain amino acid sequence of SEQ ID NO: 51 with the tyrosine at CDR-L1 sulfated,
wherein the non-CDR-L1 tyrosine sulfated anti-hLAG3 antibodies and CDR-L1 tyrosine sulfated anti-hLAG3 antibodies are expressed from Chinese Hamster Ovary Cells, and wherein the purified composition is obtained by a method comprising the steps of: applying an aqueous mixture comprising CDR-L1 tyrosine sulfated and non-CDR-L1 tyrosine sulfated anti-hLAG3antibodies at a pH of about 6.5 to 7.0 to an anion exchange resin, and collecting a non-resin bound aqueous fraction of the aqueous mixture.
2. The purified composition of claim 1 , wherein the non-CDR-L1 tyrosine sulfated and CDR-L1 tyrosine sulfated anti-hLAG3 antibodies comprise N-linked glycans of one or more of G0, GO-F, G1, G1-F, G2-F and Man5 from expression in Chinese Hamster Ovary (CHO) cells.
3. The purified composition of claim 2 , wherein the non-CDR-L1 tyrosine sulfated anti-hLAG3 antibodies are glycosylated antibody species having a molecular weight of about 148590 Da, 148749 Da, 148752 Da, 148914 Da or 148915 Da, or a combination thereof.
4. The purified composition of claim 1 , wherein the non-CDR-L1 tyrosine sulfated and CDR-L1 tyrosine sulfated anti-hLAG3 antibodies have the N-terminal heavy chain glutamine converted to pyroglutamate or pyroglutamic acid and/or C-terminal heavy chain lysine removed.
5. The purified composition of claim 1 , wherein the method further comprises the following steps: washing the anion exchange resin with an aqueous composition under isocratic conditions, collecting a flow-through fraction from the wash, and pooling the flow-through fraction from the wash with the non-resin bound aqueous fraction.
6. The purified composition of claim 1 , wherein the purified composition is obtained by equilibrating the anion exchange resin comprising a dimethylaminopropyl anion exchange ligand in a chromatography column with 25 mM sodium phosphate at a pH of 6.5, adjusting the pH of the aqueous mixture to 6.5, applying the aqueous mixture to the column, collecting a flow-through fraction from the column, washing the resin in the column with 25 mM sodium phosphate at a pH of 6.5, collecting the flow-through fraction from the wash, and pooling the flow-through fractions from the aqueous mixture and the wash.
7. The purified composition of claim 1 , wherein the purified composition is obtained by equilibrating the anion exchange resin comprising a quarternized polyethyleneimine anion exchange ligand in a chromatography column with 25 mM sodium phosphate and 5 mM NaCl at a pH of 7.0, adjusting the pH of the aqueous mixture to 7.0,applying the aqueous mixture to the column, collecting a flow-through fraction from the column, washing the resin in the column with 25 mM sodium phosphate and 5 mM NaCl at a pH of 7.0,and collecting the flow-through fraction from the wash, and pooling the flow-through fractions from the aqueous mixture and the wash.
8. The purified composition of claim 7 , wherein the A280absorbance of the flow-through fraction from the aqueous mixture and wash is collected from when the A280 first reaches at least about 2.5 absorbance units/cm and continues until the A280falls below about 1.0 absorbance units/cm.
9. The purified composition of claim 6 , further comprising purifying the non-CDR-L1 tyrosine sulfated and CDR-L1 tyrosine sulfated anti-hLAG3antibodies from the pooled flow-through fractions by cation exchange chromatography, anion exchange chromatography in bind-elute mode, hydrophobic interaction chromatography, protein-A chromatography, protein-L chromatography, protein-G chromatography, hydroxyapatite chromatography, size exclusion chromatography, fractional precipitation, filtration, centrifugation or viral inactivation.
10. The purified composition of claim 6 , wherein the non-CDR-L1 tyrosine sulfated and CDR-L1 tyrosine sulfated anti-hLAG3 antibodies comprise N-linked glycans of one or more of G0, G0-F, G1, G1-F, G2-F and Man5 from expression in Chinese Hamster Ovary (CHO) cells.
11. A purified composition comprising non-CDR-L1 tyrosine sulfated antibodies that specifically bind to human lymphocyte activation gene 3 (anti-hLAG3) comprising: a heavy chain amino acid sequence of SEQ ID NO: 52 and a light chain amino acid sequence of SEQ ID NO: 51 and less than about 0.5% CDR-L1 tyrosine sulfated anti-hLAG3antibodies as compared to non-CDR-L1 tyrosine sulfated anti-hLAG3 antibodies as determined by mass spectrometry, wherein the CDR-L1 tyrosine sulfated anti-hLAG3 antibodies comprise a heavy chain amino acid sequence of SEQ ID NO: 52 and a light chain amino acid sequence of SEQ ID NO: 51 with the tyrosine at CDR-L1 sulfated, wherein the non-CDR-L1 tyrosine sulfated anti-hLAG3 antibodies and the CDR-L1 tyrosine sulfated anti-hLAG3 antibodies are expressed from Chinese Hamster Ovary Cells, and wherein the purified composition is obtained by a method comprising the steps of: applying an aqueous mixture comprising CDR-L1 tyrosine sulfated and non-CDR-L1 tyrosine sulfated anti-hLAG3 antibodies at a pH of 6.5 to 7.5 to an anion exchange resin, and collecting a non-resin bound aqueous fraction of the aqueous mixture.
12. The purified composition of claim 11 , wherein the method further comprises the following steps: washing the anion exchange resin with an aqueous composition under isocratic conditions, collecting a flow-through fraction from the wash, and pooling the flow-through fraction from the wash with the non-resin bound aqueous fraction.
13. The purified composition of claim 11 , wherein the purified composition is obtained by equilibrating the anion exchange resin with about 10-50 mM sodium phosphate at a pH of 6.5 to 7.5, adjusting the pH of the aqueous mixture to 6.5 to 7.5, applying the aqueous mixture to the column, collecting a flow-through fraction from the column, washing the resin in the column with about 10-50 mM sodium phosphate at a pH of 6.5 to 7.5, and collecting a flow-through fraction from the wash, and pooling the flow-through fractions from the aqueous mixture and the wash.
14. The purified composition of claim 11 , wherein the non-CDR-L1 tyrosine sulfated and CDR-L1 tyrosine sulfated anti-hLAG3 antibodies comprise a heavy chain amino acid sequence of SEQ ID NO: 52 and a light chain amino acid sequence of SEQ ID NO: 51 with the N-terminal heavy chain glutamine converted to pyroglutamate or pyroglutamic acid and/or the C-terminal heavy chain lysine removed.
15. The purified composition of claim 14 , wherein the non-CDR-L1 tyrosine sulfated anti-hLAG3 antibodies are glycosylated antibody species having molecular weights of about 148590 Da, 148749 Da, 148752 Da, 148914 Da, or 148915 Da, or a combination thereof.
16. The purified composition of claim 11 , wherein the non-CDR-L1 tyrosine sulfated and CDR-L1 tyrosine sulfated anti-hLAG3 antibodies comprise N-linked glycans of one or more of G0, G0-F, G1, G1-F, G2-F and Man5 from expression in Chinese Hamster Ovary (CHO) cells.
17. The purified composition of claim 14 , wherein the non-CDR-L1 tyrosine sulfated and CDR-L1 tyrosine sulfated anti-hLAG3 antibodies comprise N-linked glycans of one or more of G0, G0-F, G1, G1-F, G2-F and Man5 from expression Chinese Hamster Ovary (CHO) cells.
18. The purified composition of claim 10 , wherein the non-CDR-L1 tyrosine sulfated anti-hLAG3 antibodies are glycosylated antibody species having a molecular weight of about 148590 Da, 148749 Da, 148752 Da, 148914 Da, 148915 Da, or a combination thereof.
19. The purified composition of claim 18 , wherein the non-CDR-L1 tyrosine sulfated anti-hLAG3 antibodies have: (i) a molecular weight of 148590 Da, (ii) G0F glycans, (iii) the N-terminal heavy chain glutamine converted to pyroglutamic acid, and (iv) the C-terminal heavy chain lysine removed.
20. The purified composition of claim 18 , wherein the non-CDR-L1 tyrosine sulfated anti-hLAG3 antibodies have: (i) a molecular weight of 148749 Da or 148752 Da, (ii) GOP and G1F glycans, (iii) the N-terminal heavy chain glutamine converted to pyroglutamic acid, and (iv) the C-terminal heavy chain lysine removed.
21. The purified composition of claim 18 , wherein the non-CDR-L1 tyrosine sulfated anti-hLAG3 antibodies have: (i) a molecular weight of 148914 Da or 148915 Da, (ii) G1F glycans, (iii) the N-terminal heavy chain glutamine converted to pyroglutamic acid, and (iv) the C-terminal heavy chain lysine removed.
22. The purified composition of claim 15 , wherein the non-CDR-L1 tyrosine sulfated anti-hLAG3 antibodies have: (i) a molecular weight of 148590 Da, (ii) G0F glycans, (iii) the N-terminal heavy chain glutamine converted to pyroglutamic acid, and (iv) the C-terminal heavy chain lysine removed.
23. The purified composition of claim 15 , wherein the non-CDR-L1 tyrosine sulfated anti-hLAG3 antibodies have: (i) a molecular weight of 148749 Da or 148752 Da, (ii) GOP and G1F glycans, (iii) the N-terminal heavy chain glutamine converted to pyroglutamic acid, and (iv) the C-terminal heavy chain lysine removed.
24. The purified composition of claim 15 , wherein the non-CDR-L1 tyrosine sulfated anti-hLAG3 antibodies have: (i) a molecular weight of 148914 Da or 148915 Da, (ii) G1F glycans, (iii) the N-terminal heavy chain glutamine converted to pyroglutamic acid, and (iv) the C-terminal heavy chain lysine removed.