Recombinant pegylated interferon for dogs, fusion protein for preparation of recombinant pegylated interferon and preparation method of recombinant pegylated interferon
A fusion protein, canine interferon technology, applied in the field of biological genetic engineering, can solve the problems of small molecular weight, short half-life, unfavorable application and the like of interferon, and achieve the effects of avoiding denaturation and renaturation, improving half-life and shortening expression time.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0075] A fusion protein composed of canine interleukin 2 and canine interferon α, the preparation method of which is as follows:
[0076] 1. Acquisition and amplification of canine interleukin-2 (IL-2) and canine interferon-α (IFN-α) target genes
[0077] Primer design:
[0078] Design synthetic primers according to the target gene sequence reported in Genebank, see Table 1, introduce BamHI restriction site and Linker sequence into the upstream primer and downstream primer of canine interleukin 2, respectively, and introduce the upstream primer and downstream primer of canine interferon α Linker sequence and XhoI restriction site were introduced respectively.
[0079] Table 1 PCR amplification primers
[0080]
[0081] RT-PCR to obtain the target gene:
[0082] RNA was extracted from canine liver tissue, and the target genes of IL-2 and IFN-α were obtained by reverse transcription. The gene sequences of the two are shown in SEQUENCE LISTING 400 and SEQUENCE LISTING 400, ...
Embodiment 2
[0115] A fusion protein composed of canine interleukin 2 and canine interferon α, the others are 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 cell. The SDS-PAGE electrophoresis result of the fusion protein is compared with that of Example 1, and the dominant expression band at about 56.8KD in the supernatant is thicker, indicating that after the introduction of molecular chaperone pGro7, the expression of the target protein in the supernatant is better, and the 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.
[0116] The BL21(DE3) competent cells carrying the pGro7 plasmid were purchased from Shanghai Inshore Science & Technology Co., Ltd. / Simbano Biotech...
Embodiment 3
[0118] A fusion protein composed of canine interleukin 2 and canine interferon α, the preparation method of which is as follows:
[0119] 1. Acquisition and amplification of canine interleukin-2 (IL-2) and canine interferon-α (IFN-α) target genes
[0120] IL-2 and IFN-α in Example 1 are optimized, and IL-2 and IFN-α target genes are artificially synthesized. After optimization, the nucleotide sequences of the two are as SEQUENCE LISTING 400 and SEQUENCE LISTING 400 respectively As shown in .
[0121] 1.1 Codon optimization
[0122] 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, and those that are not frequently used are called rare or low-usage codons. Virtually every organism commonly used for protein expression or production (including E. coli, yeast, mammalian cells, plant cells, and insect cells) exhibits some degree of difference or bias in codon usage. The expression efficie...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com