Recombinant mite allergen protein drug mixture and application thereof
A protein drug and allergen technology, which is applied in the direction of drug combination, allergen antigen components, peptide/protein components, etc., can solve the problems of time-consuming, cumbersome process, and pathogen microbial contamination, so as to reduce antigenic epitopes, reduce Anaphylaxis, good immunogenic effect
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Embodiment 1
[0051] Example 1 Recombinant proDP1 codon optimization transformation, construction of expression plasmid and construction of host engineering strain
[0052] Step 1: Recombination codon optimization transformation
[0053] According to the DNA sequence of DP1 published by EMBL-EBI (ENA accession number: FM177224.1), the inventor obtained the proDP1 gene of the present invention (the proDP1 gene (the The gene has an alpha-factor signal peptide and a Kozak sequence GCCACCATGG added on the basis of the wild-type gene, and has been codon-optimized), and the nucleotide sequence is shown in SEQ ID No:1.
[0054] According to the DNA sequence of DF1 published by GenBank (GenBank accession number: AB034946.1), the inventor obtained the proDF1 gene of the present invention after combining the requirements of the expression system of the present invention and multiple verifications, and obtained the proDF1 gene of the present invention (the gene is in The alpha-factor signal pepti...
Embodiment 2
[0069] Example 2 Recombinant DP1 / DF1 large-scale (30L) high-density fermentation experiment
[0070] The following will first illustrate with DP1 large-scale (30L) high-density fermentation
[0071] Step 1: Activation of recombinant strains
[0072] Get the glycerol bacteria seeds produced after the above-mentioned examples and freeze them in the working seed bank at -80°C in YPD solid medium (yeast extract 10g / L, peptone 20g / L, glucose 20g / L, agarose 15g / L) Streak the line and cultivate in a constant temperature and humidity chamber at 30°C for 3-5 days.
[0073] Step 2: Primary seed liquid culture
[0074] Pick the monoclonal colonies on the plate in step 1 and culture them in YPD liquid medium (yeast extract 10g / L, peptone 20g / L, glucose 20g / L) at 30°C and 220rpm until OD 600 ≈6.0, and observed under a microscope without any bacteria, the first-grade seed liquid for fermentation was obtained.
[0075] Step 3: Secondary Seed Solution Culture
[0076] Inoculate t...
Embodiment 3
[0081] Embodiment 3 recombinant DP1 / DF1 purification process
[0082] 1. The first step of purification of recombinant DP1 / DF1 fermentation broth supernatant
[0083] Step 1: Pretreatment of the fermentation broth
[0084] The fermentation broth obtained in the above examples was centrifuged at high speed to obtain a supernatant; diatomaceous earth was added to aid in filtration, and a clarified fermentation broth sample was obtained overnight; diluted with a 10KD membrane bag ultrafiltration to reduce the conductance to below 5mS / cm.
[0085] Step 2: Cation Exchange Chromatography
[0086] The acetic acid of the fermented liquid supernatant after the above treatment is adjusted to pH 4.0, and put on the SP FF chromatography column. 50mM NaAc, 1.0M NaCl, pH4.0, according to 0-100% linear elution, DP1 / DF1 target protein is mainly concentrated in the second elution peak.
[0087] The rest of the conditions remained unchanged, and the pH of the sample and buffer was adjust...
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