Methods for purifying antibodies
A method for purifying a protein comprising an antibody, antibody fragment, or immunoglobulin single variable domain, from a solution containing at least one contaminant by superantigen chromatography comprising: a) adsorbing the protein to the superantigen immobilized on a solid support; b) removing the at least one contaminant by contacting the immobilized superantigen containing the adsorbed protein with a first wash buffer comprising an aliphatic carboxylate; and c) eluting the protein from the superantigen immobilized on the solid support.
1. A method for purifying a protein from a solution by superantigen chromatography comprising:
a) adsorbing the protein to the superantigen immobilized on a solid support;
b) removing at least one contaminant by contacting the immobilized superantigen containing the adsorbed protein with a first wash buffer comprising 50 mM to 125 mM sodium caprylate; and
c) eluting the protein from the superantigen immobilized on the solid support,
wherein the solution comprises the protein and the at least one contaminant,
wherein the solution is a cell culture feed stream, and
wherein the at least one contaminant is selected from the group consisting of a host cell protein and host cell DNA.
2. The method of claim 1 , wherein the first wash buffer comprises 50 mM to 100 mM sodium caprylate.
3. The method of claim 1 , wherein the first wash buffer comprises 50 mM to 75 mM sodium caprylate.
4. The method of claim 1 , wherein the first wash buffer comprises 75 mM to 125 mM sodium caprylate.
5. The method of claim 1 , wherein the first wash buffer comprises 75 mM to 100 mM sodium caprylate.
6. The method of claim 1 , wherein the superantigen is selected from the group consisting of Protein A, Protein G, and Protein L.
7. The method of claim 1 , wherein the wash buffer further comprises 100 mM to 400 mM sodium acetate.
8. The method of claim 1 , wherein the protein is selected from the group consisting of soluble receptor, antibody, antibody fragment, immunoglobulin single variable domain, Fab, F(ab′)2, Fv, disulphide linked Fv, scFv, closed conformation multispecific antibody, disulphide-linked scFv, and diabody.
9. The method of claim 1 , wherein the host cell is selected from the group consisting of E. coli cells, CHO cells, NS0 cells, Sp2/0 cells, COS cells, K562 cells, BHK cells, PER.C6 cells, and HEK cells.
10. The method of claim 1 , wherein the wash buffer further comprises one selected from the group consisting of an organic acid, an alkaline metal salt of the conjugate base of the organic acid, an ammonium salt of the conjugate base of the organic acid, and an organic base.
11. The method of claim 10 , wherein the organic acid is selected from the group consisting of formic acid, acetic acid, lactic acid, citric acid, malic acid, maleic acid, glycine, glycylclycine, succinic acid, TES (2-{[tris(hydroxymethyl)methyl]amino}ethanesulfonic acid), MOPS (3-(N-morpholino)propanesulfonic acid), PIPES (piperazine-N,N′-bis(2-ethanesulfonic acid)), and MES (2-(N-morpholino)ethanesulfonic acid); and wherein the organic base is selected from the group consisting of tris base, Bis-tris, Bis-tris-Propane, Bicine (N,N-bis(2-hydroxyethyl)glycine), HEPES (4-2-hydroxyethyl-1-piperazineethanesulfonic acid), TAPS (3-{[tris(hydroxymethyl)methyl]amino}propanesulfonic acid), and Tricine (N-tris(hydroxymethyl)methylglycine).
12. The method of claim 10 , wherein the conjugate base of the organic acid is one selected from the group consisting of the sodium salt of the conjugate base of the organic acid, the potassium salt of the conjugate base of the organic acid, and the ammonium salt of the conjugate base of the organic acid.
13. A method for purifying a protein from a contaminated solution comprising:
(a) equilibrating Protein A immobilized on a solid phase with Protein A equilibration buffer or equilibrating Protein L immobilized on a solid phase with Protein L equilibration buffer;
(b) adsorbing the protein from the contaminated solution to the Protein A or Protein L immobilized on the solid phase;
(c) removing at least one contaminant by washing the solid phase with a first Protein A or a first Protein L wash buffer comprising 50 mM to 55 mM tris base, 45 mM to 50 mM acetic acid, 50 mM to 125 mM sodium caprylate, and
(d) recovering the protein from the solid phase with a Protein A elution buffer or a Protein L elution buffer,
wherein the contaminated solution comprises the protein and the at least one contaminant,
wherein the contaminated solution is a cell culture feed stream, and
wherein the at least one contaminant is selected from the group consisting of a host cell protein and host cell DNA.
14. The method of claim 13 , further comprising the following step after step (c) and before step (d): removing contaminants by washing the solid phase with a second Protein A wash buffer comprising 55 mM tris base, 45 mM acetic acid, at pH 7.2.
15. The method of claim 13 , further comprising the following steps after step (d): (e) titrating the solution containing the recovered protein to pH 3.0 with 30 mM acetic acid, 100 mM HCl; (f) allowing the solution of step (e) to remain at pH 3.0 for about 30 to 60 minutes; and (g) adjusting the pH of the solution of step (f) to pH 7.5 with 1 M tris.
16. The method of claim 13 , wherein the Protein A wash buffer or the Protein L wash buffer further comprises 1 mM to about 500 mM sodium acetate.
17. The method of claim 13 , wherein the protein is selected from the group consisting of soluble receptor, antibody, antibody fragment, immunoglobulin single variable domain, Fab, F(ab′)2, Fv, disulphide linked Fv, scFv, closed conformation multispecific antibody, disulphide-linked scFv, and diabody.
18. The method of claim 1 , wherein the protein is expressed by the host cell.
19. The method of claim 13 , wherein the protein is expressed by the host cell.
20. The method of claim 15 , further comprising filtering the solution produced by step (g).