Long-acting recombinant human follicle-stimulating hormone-Fc fusion protein (hFSH-Fc)
A fusion protein, hfsh-fc technology, applied in its preparation method and application, in the field of long-acting recombinant human follicle-stimulating hormone fusion protein, can solve the problems of low expression of recombinant hFSH, short half-life in vivo, difficult purification, etc., to achieve no immunity Originality, prolonging the half-life in vivo, and improving the effect of biological activity
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Embodiment 1
[0067] Example 1. Construction of gene expression vector encoding recombinant hFSH-Fc fusion protein
[0068] The gene sequence design was optimized based on the preferred codons of CHO cells, and the optimized fusion gene containing the signal peptide encoding hFSH protein β chain and its mature peptide, CTP and hFSH α chain mature peptide was synthesized by artificial synthesis. The synthetic 756bp DNA fragment was inserted between the EcoRV restriction sites in the transfer vector such as pUC57 to obtain the hFSH plasmid (phFSH), and the correctness of the inserted sequence was verified by DNA sequencing.
[0069] The fusion gene L- that encodes a flexible peptide linker (Linker, referred to as "L") and human IgG Fc variants (vIgG4Fc and vIgG1Fc) fragments containing BamHI (5' end) and EcoRI (3' end) restriction sites was artificially synthesized, respectively. vIgG4Fc and L-vIgG1Fc. The obtained fusion gene fragments were respectively inserted between the BamHI and EcoRI ...
Embodiment 2
[0072] Example 2. Stable expression of recombinant hFSH-Fc fusion protein in mammalian cells
[0073] The expression plasmid pCDNA3-hFSH-L-Fc constructed in Example 1 was transfected into DHFR enzyme-deficient CHO host cells (CHO-DHFR - ), figure 2 b shows a schematic diagram of the recombinant dimerized hFSH-Fc fusion protein. Transfection was carried out by electroporation, using a Gene Pulser Electroporator (Bio-Rad Laboratories, Hercules, CA) with a capacitance of 960 μFd, setting its electric field to 250 V, and using 2 to 5 × 10 cells in the cuvette. 7 Add 10 μg of plasmid DNA linearized with PvuI to each cell. Two days after transfection, the medium was changed to a growth medium containing 100 μg / mL Zeocin resistance marker gene to obtain transfectants that had passed the initial resistance screening. The expression of hFSH-Fc was detected with anti-hFSH antibody by westernblotting method. The use of DHFR to amplify the selectable marker gene increases the express...
Embodiment 3
[0074] Example 3. Production and purification of recombinant hFSH-Fc fusion protein
[0075] The high-yield cell strain obtained in Example 2 was first acclimatized in a culture dish without serum, and then transferred to a shake flask for suspension acclimatization. During the acclimatization process, the medium was screened at the same time, and different components were added to observe the growth of the cells. Growth state, growth trend, and biochemical indicators such as the activity of the expressed product and sialic acid, the preferred cell culture conditions are: basal medium with 100 μM Cu 2+ , adding 2mM ManNAc (N-acetyl-D-aminomannose) to the feeding medium, this method can increase the glycosylation degree of the recombinant hFSH-Fc fusion protein, and increase the sialic acid content by about 20%. After the acclimatization is successful, the cells are expanded to a sufficient amount, and the 7L bioreactor is monitored for culture. When the cell density exceeds 1×...
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