Protein production method
This invention relates to a method for producing a protein of interest, comprising introducing a protein expression vector which comprises a gene fragment a gene fragment comprising a DNA encoding a protein of interest and a selectable marker gene and transposon sequences at both terminals of the gene fragment, into a suspension mammalian cell; integrating the gene fragment inserted between a pair of the transposon sequences, into a chromosome of the mammalian cell to obtain a mammalian cell capable of expressing the protein of interest; and suspension-culturing the mammalian cell; and a suspension mammalian cell capable of expressing the protein of interest.
1. A method selected from the group consisting of (I) and (II):
(I) a method for increasing expression of a protein of interest, comprising introducing an expression vector which comprises a gene fragment comprising a DNA encoding the protein and a selectable marker gene, and transposon sequences at both terminals of the gene fragment, into a suspension mammalian cell; integrating the gene fragment inserted between a pair of the transposon sequences, into a chromosome of the mammalian cell to obtain a mammalian cell capable of expressing the protein; and suspension-culturing the mammalian cell; or
(II) a method for increasing expression of a protein of interest, which comprises the following steps (A) to (C):
(A) a step of simultaneously introducing the following expression vectors (a) and (b) into a suspension mammalian cell,
(a) an expression vector which comprises a gene fragment comprising a DNA encoding the protein, and transposon sequences at both terminals of the gene fragment,
(b) an expression vector which comprises a DNA encoding a transposase which recognizes the transposon sequences and has activity of transferring a gene fragment inserted between a pair of the transposon sequences into a chromosome,
(B) a step of transiently expressing the transposase from the expression vector introduced in the step (A) to integrate the gene fragment inserted between a pair of the transposon sequences into a chromosome of the mammalian cell, to obtain a suspension mammalian cell capable of expressing the protein, and
(C) a step of suspension-culturing the suspension mammalian cell capable of expressing the protein obtained in step (B);
wherein in the methods of (I) or (II), the pair of transposon sequences are nucleotide sequences derived from a pair of Tol1 transposons or nucleotide sequences derived from a pair of Tol2 transposons, and
wherein the suspension mammalian cell is at least one selected from a suspension CHO cell in which a CHO cell is adapted to suspension culture, a PER.C6 cell, a rat myeloma cell YB2/3HL.P2.G11.16Ag.20 (or YB2/0) and a suspension mouse myeloma cell NS0 adapted to suspension culture.
2. The method according to claim 1 ,
(I) wherein the suspension mammalian cell is a cell capable of surviving and proliferating in a serum-free medium;
(II) wherein the selectable marker gene is a cycloheximide resistance gene; and/or
(III) wherein the pair of transposon sequences are nucleotide sequences derived from a pair of DNA-type transposons which function in a mammalian cell.
3. The method according to claim 1 , wherein the CHO cell is at least one selected from CHO-K1, CHO-K1SV, DUKXB11, CHO/DG44, Pro-3 and CHO-S.
4. The method according to claim 2 , wherein the cycloheximide resistance gene is a gene encoding a mutant of human ribosomal protein L36a.
5. The method according to claim 4 , wherein the mutant is a mutant in which proline at position 54 of the human ribosomal protein L36a is substituted with other amino acid.
6. The method according to claim 5 , wherein the other amino acid is glutamine.
7. The method according to claim 1 ,
(I) wherein the nucleotide sequences derived from a pair of Tol2 transposons are a nucleotide sequence comprising the nucleotide sequence shown in SEQ ID NO:2 and the nucleotide sequence shown in SEQ ID NO:3; or
(II) wherein the nucleotide sequences derived from a pair of Tol1 transposons are the nucleotide sequence shown in SEQ ID NO:14 and the nucleotide sequence shown in SEQ ID NO:15.
8. A suspension mammalian cell capable of increasing expression of a protein of interest,
(I) into which an expression vector comprising a gene fragment comprising a DNA encoding the protein and a selectable marker gene, and transposon sequences at both terminals of the gene fragment is introduced, to integrate the gene fragment inserted between a pair of the transposon sequences into a chromosome; or
(II) into which an expression vector (a) comprising a gene fragment comprising a DNA encoding the protein and a selectable marker gene, and transposon sequences at both terminals of the gene fragment, and an expression vector (b) comprising a DNA encoding a transposase which recognizes the transposon sequences and has activity of transferring the gene fragment inserted between a pair of the transposon sequences into a chromosome to integrate the gene fragment inserted between a pair of the transposon sequences into the chromosome,
wherein in the methods of (I) or (II), the pair of transposon sequences are nucleotide sequences derived from a pair of Tol1 transposons or nucleotide sequences derived from a pair of Tol2 transposons, and
wherein the suspension mammalian cell is at least one selected from a suspension CHO cell in which a CHO cell is adapted to suspension culture, a PER.C6 cell, a rat myeloma cell YB2/3HL.P2.G11.16Ag.20 (or YB2/0) and a suspension mouse myeloma cell NS0 adapted to suspension culture.
9. The cell according to claim 8 ,
(I) wherein the cell is a cell capable of surviving and proliferating in a serum-free medium;
(II) wherein the selectable marker gene is a cycloheximide resistance gene; and/or
(III) wherein the pair of transposon sequences are nucleotide sequences derived from a pair of DNA type transposons which function in a mammalian cell.
10. The cell according to claim 9 , wherein the CHO cell is at least one selected from CHO-K1, CHO-K1SV, DUKXB11, CHO/DG44, Pro-3 and CHO-S.
11. The cell according to claim 9 , wherein the cycloheximide resistance gene is a gene encoding a mutant of human ribosomal protein L36a.
12. The cell according to claim 11 , wherein the mutant is a mutant in which proline at position 54 of the human ribosomal protein L36a is substituted with other amino acid.
13. The cell according to claim 12 , wherein the other amino acid is glutamine.
14. The cell according to claim 8 ,
(I) wherein the nucleotide sequences derived from a pair of Tol2 transposons are the nucleotide sequence shown in SEQ ID NO:2 and the nucleotide sequence shown in SEQ ID NO:3; or
(II) wherein the nucleotide sequences derived from a pair of Tol1 transposons are the nucleotide sequence shown in SEQ ID NO:14 and the nucleotide sequence shown in SEQ ID NO:15.
15. The expression vector for increasing expression of a protein of interest according to claim 1 or 8 , comprising a gene fragment comprising a DNA encoding a protein of interest and a selectable marker gene, and a pair of transposon sequences at both terminals of the gene fragment; and
wherein the pair of transposon sequences are nucleotide sequences derived from a pair of Tol1 transposons or nucleotide sequences derived from a pair of Tol2 transposons.
16. The expression vector according to claim 15 ,
(I) wherein the nucleotide sequences derived from a pair of the Tol2 transposons are the nucleotide sequence shown in SEQ ID NO:2 and the nucleotide sequence shown in SEQ ID NO:3; or
(II) wherein the nucleotide sequences derived from a pair of the Tol1 transposons are the nucleotide sequence shown in SEQ ID NO:14 and the nucleotide sequence shown in SEQ ID NO:15.