Bovine rotavirus fusion protein and calf diarrhea polyvalent vaccine
A bovine rotavirus and fusion protein technology, which is applied in the field of bovine rotavirus fusion protein and calf diarrhea multiple vaccines, to achieve good immunogenicity, expand the scope of disease prevention and control, and save labor
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[0064] In some optional embodiments, taking yeast as the host cell as an example, the preparation method includes the steps of gene preparation, recombinant vector construction, cell transfection, high-efficiency expression strain screening, and recombinant protein acquisition, specifically including: The obtained vector is linearized and electrotransformed into yeast competent cells, the fusion protein is expressed, and the fusion protein is purified to obtain the fusion protein. Then, an appropriate buffer is selected to assemble the purified fusion protein for virus-like particles, and the assembly effect is identified by electron microscope. The vector preferably uses the pPIC3.5K vector. After the linearized vector is electrotransformed into yeast competent cells, it is preferably directly coated on a high antibiotic concentration plate, and high selection pressure is used to select high expression monoclonal strains. The electrotransformation preferably uses multiple elec...
Embodiment 1
[0070] Express the fusion protein through the Pichia pastoris expression system:
[0071] By means of structural biology, the structure of the bovine rotavirus VP6 protein was analyzed, and the epitopes of bovine coronavirus and pathogenic E. coli were chimerized into the bovine rotavirus VP6 protein backbone, and the sequence was named VP6-S -K88 / K99, the specific amino acid sequence is shown in SEQ ID NO. 8;
[0072] The fusion protein VP6-S-K88 / K99 was codon optimized for Pichia pastoris expression system, and the nucleotide sequence is shown in SEQ ID NO.9.
[0073] And by means of genetic engineering, the gene encoding the VP6-S-K88 / K99 fusion protein was synthesized, and the target gene and pPIC3.5k plasmid were digested with Bam HI and AgeI respectively (restriction system: 1μg plasmid, 1μL Bam HI, 1μL Age I, 5μL CutSmart, ddH 2 O fill up to 50μL; incubate at 37°C for 1h), recover the band of interest through a 1% agarose gel (Axyprep DNA Gel Recovery Kit AP-GX-250), measure ...
Embodiment 2
[0079] To express multi-layer chimeric VLP particles through the Pichia pastoris expression system:
[0080] By means of genetic engineering, the gene encoding VP2-N93 protein was synthesized, and the amino acid sequence is shown in SEQ ID NO.10. The target gene and pPICZ A vector were digested with Bst BI and Age I respectively (restriction system: 1μg plasmid, 1μL BstBI, 1μL Age I, 5μL CutSmart, ddH 2 O fill up to 50μL; incubate at 37°C for 1h), recover the target bands by 1% agarose gel (Axyprep DNA Gel Recovery Kit AP-GX-250), and measure the concentrations respectively, and then use T4 DNA Ligase (NEB , M0202) Connect the vector to the gene, mix the ligation system with E.Coli DH5α competent cells, incubate on ice for 30 minutes, then place at 42°C for 90 seconds, then immediately place on ice for 2 minutes, and apply directly to 0.1mg / mL ampicillin Plate, culture at 37°C for 16h, pick a single clone into 2mL LB medium and culture for 16h, extract the plasmid by Axgen kit (A...
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