Small molecule recombination toxin GnRH-luffinS2 fusion albumen and its preparation and application
A fusion protein and hormone-releasing technology, applied in drug combination, peptide/protein components, recombinant DNA technology, etc., can solve the problem of difficult to accurately control the location and degree of sulfhydrylation, space hindrance of receptors and ligands, and generation of heterologous molecules problems such as low immunogenicity, small molecular weight, and high-efficiency expression
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Embodiment 1
[0032] Example 1 PCR Amplification of GnRH-luffin S2 Recombinant Fragment
[0033] Use the Codon software package to design 6 overlapping PCR primers, use overlapping PCR to amplify the GnRH-luffin S2 fragment, and add BamHI and HindIII restriction sites to both ends of the first primer and the last primer respectively. Each primer is shown in the sequence list SEQ ID NO.1~NO.6.
Embodiment 2
[0034] Example 2 Connection of GnRH-luffin S2 amplified fragment and expression vector pQE-30
[0035] GnRH-luffin S2 and pQE-30 were digested with BamHI and HindIII respectively, recovered and ligated to obtain pQE / GnRH-luffin S2, whose sequence is shown in SEQ ID NO.7 in the sequence list.
Embodiment 3
[0036] Example 3 Expression of Fusion Gene
[0037] Transform into Escherichia coli M15 for expression, the specific conditions are: Inoculate the Escherichia coli strain containing the expression plasmid into LB medium, shake overnight at 37°C, inoculate fresh LB medium at 1:100 the next day, shake at 37°C to OD 600 =0.4, add the inducer IPTG, the concentration is 0.4mM, continue to shake at 37°C for 5 hours, induce the production of GnRH-luffin S2 fusion protein, its sequence is as SEQ ID NO.8 in the sequence listing.
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