Fusion protein composed of sheep albumin, interferon Tau and interleukin 2, preparation method thereof and its coding gene, and sheep long-acting interferon
A technology of fusion protein and interferon, which is applied in the direction of interferon, biochemical equipment and methods, cytokines/lymphokines/interferon, etc., and can solve problems such as unfavorable clinical application, high cost of interferon, and small molecular weight of interferon
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Embodiment 1
[0092] The preparation method of ovine albumin-interferon tau-interleukin 2 fusion protein comprises the following steps:
[0093] 1. Acquisition and amplification of sheep albumin (Alb), sheep interferon τ (IFN-τ) and sheep interleukin 2 (IL-2) target genes
[0094] Primer design:
[0095] Synthetic primers were designed and synthesized according to the target gene sequence reported in Genebank, as shown in Table 1. The EcoRI restriction site was introduced into the upstream primer of ovine albumin, the Linker sequence was introduced into the downstream primer, and the upstream primer and downstream primer of ovine interferon τ The Linker sequence was introduced into the upstream primer of sheep interleukin 2, and the Linker sequence was introduced into the downstream primer, and a SalI restriction site was introduced into the downstream primer.
[0096] Table 1 PCR amplification primers
[0097]
[0098] RT-PCR to obtain the target gene:
[0099] RNA was extracted from...
Embodiment 2
[0135] A method for preparing ovine albumin-interferon τ-interleukin 2 fusion protein, the preparation method is the same as in Example 1, except that the Escherichia coli BL21 (DE3) competent cells are replaced by BL21 (DE3) competent cells with pGro7 plasmid state cells. The SDS-PAGE electrophoresis result of the fusion protein is compared with that of Example 1. The dominant expression band at about 125.9KD in the supernatant is relatively thick, indicating that after the introduction of the molecular chaperone pGro7, the expression of the target protein in the supernatant is better, and it is obtained The amount of fusion protein is higher. Most of the proteins expressed in E. coli exist in inclusion bodies; by introducing molecular chaperones into the expression strains, the co-expressed proteins can be correctly folded to achieve protein soluble expression.
[0136] The BL21(DE3) competent cells carrying the pGro7 plasmid were purchased from Shanghai Inshore Science & T...
Embodiment 3
[0139] A method for preparing ovine albumin-interferon tau-interleukin 2 fusion protein, the preparation method is as follows:
[0140]1. Acquisition and amplification of sheep albumin (Alb), sheep interferon τ (IFN-τ) and sheep interleukin 2 (IL-2) target genes
[0141] Goat Alb, goat IFN-τ and goat IL-2 in Example 1 were optimized, and goat Alb, goat IFN-τ and goat IL-2 target genes were artificially synthesized. After optimization, the nucleotide sequences of the three were as follows: SEQUENCE LISTING 400, SEQUENCELISTING 400 and SEQUENCE LISTING 400.
[0142] 1.1 Codon optimization
[0143] There are 64 genetic codes, but most organisms tend to use a subset of these. Those that are most frequently used are called optimal codons (opτimal codons), and those that are not frequently used are called rare or low-usage codons (rare or low-usage codons). Virtually every organism commonly used for protein expression or production (including E. coli, yeast, mammalian cells, plan...
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