Recombined human gama interferon gland virus and preparation of products therefrom
An adenovirus and interferon technology, applied in the field of genetic engineering, can solve the problems of unstable nature and easy inactivation, and achieve the effects of high titer, stable and lasting expression, and wide host range
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Embodiment 1
[0036] Recombinant human γ-interferon adenovirus (Ad-rhIFNγ) contains secreted human γ-interferon target gene and defective adenovirus. The defective adenovirus is adenovirus type 5 of subgroup C (Ad5).
[0037] Ad-hIFN-γ structure: the recombinant human γ-interferon adenoviral vector has deleted the E1 region (E1 Δ ), and part of the E3 region (partiteE3 Δ ), the human γ-interferon protein gene is the target gene, and the expression cassette expressing secreted human γ-interferon is inserted into the E1 region. The target gene expression cassette is composed of cell virus (CMV) promoter, human γ-interferon gene and Downstream polyA signaling components (see figure 1 ).
Embodiment 2
[0039] Preparation of recombinant human gamma-interferon adenovirus:
[0040] The production process of recombinant human γ-interferon adenovirus includes: construction of plasmid, transfection of bacteria, infection of 293 cells, separation and purification, etc. Specifically see its production process flow chart (see figure 2 ).
Embodiment 3
[0042] Expression detection of recombinant human gamma-interferon adenovirus target gene:
[0043] 1. Inoculate C6 cells into a 96-well plate, 2×10 4 / hole.
[0044] 2. After 24 hours, inoculate Ad-hIFN-γ. Method: Dilute the virus stock solution by 4 times with 1640 culture solution. When inoculating, first suck out the culture solution in the 96-well plate and discard it. After washing the wells with PBS once, add viruses of different dilutions. solution, add 6 wells for each dilution, 50 μL / well. At the same time, 1640 culture medium (without virus) was used as negative control. 37°C, 5% CO 2 , after incubating for 1 hour under saturated humidity conditions, add 1640 culture solution containing 5% newborn calf serum, 200 μL / well, 37 ° C, 5% CO 2 , cultivated under saturated humidity conditions.
[0045] 3. After that, collect the cell supernatant in 2 wells of each dilution every 24 hours, store at -80°C, and collect 3 times in a row.
[0046] 4. According to the instr...
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