Method for the production of fusion proteins in transgenic mammal milk
View Patent ↗Desirable fusion proteins can be produced in and purified from the milk of transgenic animals. The peptides are made as fusion proteins with a suitable fusion partner such as human alpha-fetoprotein. The fusion partner protein acts to promote and increase the half-life of the overall molecule as well as having therapeutic effects on its own. The fusion protein is typically produced through the use of transgenic animals and can be purified away from the now the milk or other bodily fluid of such an animal by an affinity purification method. A particular advantage of producing peptides via this route, in addition to the obvious advantages of high yield and biocompatibility, is that specific post-translational modifications, such as carboxy terminal amidation, can be performed in the mammary gland. Biologically active polypeptides comprising a therapeutically active polypeptide fused to human alpha-fetoprotein fragment or a variant thereof, methods for the preparation thereof, nucleotide sequences encoding such fusion polypeptides, expression cassettes comprising such nucleotide sequences, self-replicating plasmids containing such expression cassettes, and pharmaceutical compositions containing said fusion polypeptides.
1. A bifunctional fusion protein, encoded by a transgene DNA construct, comprising a human alpha-fetoprotein and human interferon-beta (IFN-β).
2. The fusion protein of claim 1 , wherein said fusion protein is the product of a contiguous coding sequence of DNA.
3. The fusion protein of claim 1 , further comprising a glutathione S-transferase polypeptide sequence.
4. An isolated polynucleotide encoding a bifunctional fusion protein with the amino acid sequence shown in SEQ ID NO: 4 linked to SEQ ID NO: 10.
5. A recombinant DNA vector comprising the nucleic acid sequence of the fusion protein of claim 1 .
6. A host cell transformed with said recombinant DNA vector of claim 5 .
7. A recombinant DNA vector comprising the nucleic acid sequence of the fusion protein of claim 1 , wherein said vector is an expression vector comprising a promoter operably linked to the nucleic acid sequence.
8. The fusion protein of claim 1 , wherein said DNA construct encoding said fusion protein is actuated by at least one beta-casein promoter.
9. A fusion protein produced by a method comprising:
(a) expressing the fusion protein of claim 1 by a cell; and
(b) recovering the protein.
10. The fusion protein of claim 9 , wherein said fusion protein further comprises an N-terminal methionine.
11. The fusion protein of claim 9 , wherein said fusion protein is expressed by a prokaryotic cell.
12. The fusion protein of claim 9 , wherein said fusion protein is expressed by a bacteria.
13. The fusion protein of claim 9 , wherein said fusion protein is expressed by a eukaryotic cell.
14. The fusion protein of claim 9 , wherein said fusion protein is expressed by an animal cell.
15. The fusion protein of claim 14 , wherein said animal cell is a CHO cell.
16. The fusion protein of claim 14 , wherein said animal cell is a COS cell.
17. The fusion protein of claim 9 , wherein said fusion protein is expressed by a yeast.
18. The fusion protein of claim 17 , wherein said yeast is Saccharomyces.
19. The fusion protein of claim 1 , wherein said fusion protein further comprises a peptide linker.
20. The fusion protein of claim 1 , wherein said fusion protein comprises a secretion signal sequence.
21. The fusion protein of claim 1 , wherein said human IFN-β is fused to the N-terminal end of said human alpha-fetoprotein.
22. The fusion protein of claim 1 , wherein said human IFN-β is fused to the C-terminal end of said human alpha-fetoprotein.
23. The fusion protein of claim 1 , wherein said fusion protein further comprises an amino acid linking sequence.