Method for producing antibody fusion protein

Patent metadata

Field	Value
Publication number	US-11512135-B2
Application number	US-201716327982-A
Country	US
Kind code	B2
Filing date	Aug 25, 2017
Priority date	Aug 25, 2016
Publication date	Nov 29, 2022
Grant date	Nov 29, 2022

Abstract

Disclosed is a method for production of a fusion protein in which an antibody and a lysosomal enzyme are fused. The method comprises; (a) a step of culturing mammalian cells producing the fusion protein in a serum-free medium to let the mammalian cells secrete the fusion protein in the culture medium, (b) a step of collecting culture supernatant by removing the mammalian cells from the culture medium, and (c) a step of purifying the fusion protein from the culture supernatant by using a column chromatography employing as a solid phase a material to which a substance having affinity for the fusion protein has been bound, a column chromatography employing as a solid phase a material having affinity for the phosphate group, and a size exclusion column chromatography.

First claim

The invention claimed is:

1. A method for production of a purified fusion protein in which an anti-human transferrin receptor antibody (anti-hTfR antibody) and a human iduronate-2-sulfatase (human I2S) are fused, the method comprising:
(a) culturing mammalian cells producing the fusion protein in a serum-free medium to let the mammalian cells secrete the fusion protein in the culture medium,
(b) collecting culture supernatant by removing the mammalian cells from the culture medium, and
(c) purifying the fusion protein from the culture supernatant by three column chromatography steps consisting of (i) a column chromatography employing as a solid phase a material to which a substance having affinity for the fusion protein has been bound, (ii) a column chromatography employing as a solid phase a material having affinity for the phosphate group, (iii) and a size exclusion column chromatography, wherein the three column chromatography steps (i) to (iii) are performed sequentially; wherein
said anti-hTfR antibody is a humanized antibody, and said humanized anti-hTfR antibody comprises a heavy chain and a light chain and is selected from the group consisting of (d) to (f) below;
(d) the humanized anti-hTfR antibody, wherein the light chain and the heavy chain have at least 80% amino acid sequence identity to the amino acid sequence set forth as SEQ ID NO:6 and SEQ ID NO:7, respectively,
(e) the humanized anti-hTfR antibody, wherein the light chain and the heavy chain have at least 80% amino acid sequence identity to the amino acid sequence set forth as SEQ ID NO:8 and SEQ ID NO:9, respectively, and
(f) the humanized anti-hTfR antibody, wherein the light chain and the heavy chain have at least 80% amino acid sequence identity to the amino acid sequence set forth as SEQ ID NO:10 and SEQ ID NO:11, respectively.

2. The method for production according to claim 1 , wherein the substance having affinity for the fusion protein is selected from the group consisting of Protein A, Protein G, Protein L, Protein A/G, an antigen against said antibody, an antibody recognizing said antibody as an antigen, and an antibody against the human I2S.

3. The method for production according to claim 1 , wherein the material having affinity for a phosphate group is fluoroapatite or hydroxyapatite.

4. The method for production according to claim 1 , wherein the material having affinity for phosphate group is hydroxyapatite.

5. The method for production according to claim 1 , wherein said anti-human transferrin receptor antibody and the human I2S are fused via a linker in the fusion protein, and wherein the linker is selected from the group consisting of polyethylene glycol, polypropylene glycol, copolymer of ethylene glycol and propylene glycol, polyoxyethylated polyol, polyvinyl alcohol, polysaccharide, dextran, polyvinyl ether, biodegradable polymer, lipid polymer, chitin, hyaluronic acid, biotin-streptavidin, and a derivative thereof.

6. The method for production according to claim 1 , wherein the human I2S is linked, by peptide bonds directly or via a linker sequence, to the heavy chain of said humanized anti-hTfR antibody on the C-terminal side or the N-terminal side of the heavy chain in the fusion protein.

7. The method for production according to claim 6 , wherein the linker sequence consists of 1 to 50 amino acid residues.

8. The method for production according to claim 7 , wherein the linker sequence comprises an amino acid sequence selected from the group consisting of a single glycine, a single serine, the amino acid sequence of Gly-Ser, the amino acid sequence of Gly-Gly-Ser, the amino acid sequence set forth as SEQ ID NO:1, the amino acid sequence set forth as SEQ ID NO:2, the amino acid sequence set forth as SEQ ID NO:3, and the amino acid sequences consisting of 1 to 10 thereof that are consecutively linked.

9. The method for production according to claim 7 , wherein the linker sequence is represented by the amino acid sequence of Gly-Ser.

10. The method for production according to claim 1 , wherein the human I2S is linked, by peptide bonds directly or via a linker sequence, to the light chain of said humanized anti-hTfR antibody on the C-terminal side or the N-terminal side of the light chain in the fusion protein.

11. The method for production according to claim 1 , wherein the human I2S comprises the amino acid sequence set forth as SEQ ID NO:5.

12. The method for production according to claim 1 , wherein the human I2S has at least 80% amino acid sequence identity to the amino acid sequence set forth as SEQ ID NO:5, and has an activity as human I2S.

13. The method for production according to claim 1 , wherein the human I2S has at least 90% amino acid sequence identity to the amino acid sequence set forth as SEQ ID NO:5, and has an activity as human 12S.

14. The method for production according to claim 1 , wherein the human 12S has the amino acid sequence introduced 1 to 10 amino acid substitutions, deletions or additions relative to the amino acid sequence set forth as SEQ ID NO:5, and has an activity as human 12S.

15. The method for production according to claim 1 , wherein the human 12S has the amino acid sequence introduced 1 to 5 amino acid substitutions, deletions or additions relative to the amino acid sequence set forth as SEQ ID NO:5, and has an activity as human 12S.

16. The method for production according to claim 1 , wherein the human 12S has the amino acid sequence introduced 1 to 3 amino acid substitutions, deletions or additions relative to the amino acid sequence set forth as SEQ ID NO:5, and has an activity as human 12S.

17. The method for production according to claim 1 , wherein the humanized anti-hTfR antibody is selected from the group consisting of (a) to (c) below;
(a) the humanized anti-hTfR antibody, wherein the light chain and the heavy chain thereof comprise the amino acid sequences set forth as SEQ ID NO:6 and SEQ ID NO:7, respectively,
(b) the humanized anti-hTfR antibody, wherein the light chain and the heavy chain thereof comprise the amino acid sequences set forth as SEQ ID NO:8 and SEQ ID NO:9, respectively, and
(c) the humanized anti-hTfR antibody, wherein the light chain and the heavy chain thereof comprise the amino acid sequences set forth as SEQ ID NO:10 and SEQ ID NO:11, respectively.

18. The method for production according to claim 1 , the humanized anti-hTfR antibody is selected from the group consisting of (a) to (c) below;
(a) the humanized anti-hTfR antibody, wherein the light chain and the heavy chain thereof have at least 90% amino acid sequence identity to the amino acid sequence set forth as SEQ ID NO:6 and SEQ ID NO:7, respectively,
(b) the humanized anti-hTfR antibody, wherein the light chain and the heavy chain thereof have at least 90% amino acid sequence identity to the amino acid sequence set forth as SEQ ID NO:8 and SEQ ID NO:9, respectively,
(c) the humanized anti-hTfR antibody, wherein the light chain and the heavy chain thereof have at least 90% amino acid sequence identity to the amino acid sequence set forth as SEQ ID NO:10 and SEQ ID NO:11, respectively.

19. The method for production according to claim 1 , wherein the humanized anti-hTfR antibody is selected from the group consisting of (a) to (c) below;
(a) the humanized anti-hTfR antibody, wherein the light chain thereof has the amino acid sequence introduced 1 to 10 amino acid substitutions, deletions or additions relative to the amino acid sequence set forth as SEQ ID NO:6, and wherein the heavy chain thereof has the amino acid sequence

Assignees

• Japan Chem Res

Inventors

• Koshimura Yuri
• Sonoda Hiroyuki
• Matev Miroslav
• Kakimoto Shinji
• Fukui Tsuyoshi
• Hatano Yukichi

Classifications

• C12N5/069

  Vascular Endothelial cells · CPC title

• C07K16/28

  against receptors, cell surface antigens or cell surface determinants · CPC title

• C12Y302/01017

  Lysozyme (3.2.1.17) · CPC title

• C12N15/09

  Recombinant DNA-technology · CPC title

• C12Y301/06013

  Iduronate-2-sulfatase (3.1.6.13) · CPC title