Mutant protein
View Patent ↗The present invention relates to an immunoglobulin-binding protein, wherein at least one asparagine residue has been mutated to an amino acid other than glutamine or aspartic acid, which mutation confers an increased chemical stability at pH-values of up to about 13-14 compared to the parental molecule. The protein can for example be derived from a protein capable of binding to other regions of the immunoglobulin molecule than the complementarity determining regions (CDR), such as protein A, and preferably the B-domain of Staphylococcal protein A. The invention also relates to a matrix for affinity separation, which comprises an immunoglobulin-binding protein as ligand coupled to a solid support, in which protein ligand at least one asparagine residue has been mutated to an amino acid other than glutamine.
1. In a method of separating one or more antibodies from a liquid, which method comprises:
(a) contacting said liquid with a separation matrix comprising ligands immobilised to a support;
(b) allowing antibodies to adsorb to said matrix by interaction with said ligands;
(c) optionally washing the adsorbed antibodies; and
(d) recovering antibodies by contacting said matrix with an eluent which releases the antibodies;
the improvement being a mutated protein A-based ligand having a N23T mutation in the B-domain of wild-type Staph protein A defined by SEQ ID N:1 or in protein Z defined by SEQ ID NO: 2 and further comprises a second mutation at position 43 of SEQ ID NO:2, which protein confers an increased chemical stability at alkaline pH-value.
2. The method of claim 1 , wherein the recovery of antibodies is achieved by adding an eluent having a pH in the range of 3.8-3.9.
3. The method of claim 1 , wherein at least 80% of the antibodies are recovered using an eluent having a pH in the range of 3.7-3.9.
4. The method of claim 1 , wherein at least 90% of the antibodies are recovered using an eluent having a pH in the range of 3.7-3.9.
5. The method of claim 1 , wherein at least 95% of the antibodies are recovered using an eluent having a pH in the range of 3.7-3.9.