Chromatography ligand comprising domain C from
The present invention relates to a chromatography ligand, which comprises Domain C from Staphylococcus protein A (SpA), or a functional fragment or variant thereof. The chromatography ligand presents an advantageous capability of withstanding harsh cleaning in place (CIP) conditions, and is capable of binding Fab fragments of antibodies. The ligand may be provided with a terminal coupling group, such as arginine or cysteine, to facilitate its coupling to an insoluble carrier such as beads or a membrane. The invention also relates to a process of using the ligand in isolation of antibodies, and to a purification protocol which may include washing steps and/or regeneration with alkali.
1. A chromatography ligand, which ligand comprises one or more Domain C units from Staphylococcus protein A (SpA), wherein
the Domain C sequence includes the amino acid sequence as defined by SEQ ID NO 1, with the mutation G29A or
the Domain C sequence includes the amino acid sequence as defined by SEQ ID NO 2, with the mutation G25A.
2. The ligand of claim 1 , which after 5 hours incubation in 0.5 M NaOH has retained at least 95% of its original binding capacity.
3. The ligand of claim 1 , which is capable of binding to the Fab part of an antibody.
4. The ligand of claim 1 , which further comprises a terminal coupling group, said group preferably comprising at least one nitrogen and/or sulphur atom(s).
5. The ligand of claim 4 , wherein the terminal group comprises arginine or cysteine.
6. A multimeric chromatography ligand, which contains at least two Domain C units or at least two functional fragments or variants thereof, as defined in claim 1 .
7. The ligand of claim 6 , which in addition to said at least two Domain C units, or at least two functional fragments or variants thereof, also comprises one or more other protein-based units, which are preferably alkaline-stable.
8. The ligand of claim 6 , which comprises 2-8 Domain C units, optionally coupled via linker segments.
9. A chromatography matrix comprised of ligands as defined in claim 1 coupled to at least one insoluble carrier.
10. A Fab fragment-binding chromatography matrix comprising the ligand of claim 1 coupled to at least one insoluble carrier.
11. The matrix of claim 10 , wherein the carrier is comprised of substantially spherical particles.
12. The matrix of claim 9 , wherein the carrier is porous.
13. A method of preparing a chromatography matrix, which method comprises providing ligands as defined in claim 1 ; and coupling said ligands to at least one porous carrier.
14. The method of claim 13 , wherein the coupling is carried out via a nitrogen or sulphur atom of the ligand.