Small molecular superantigen modified protein, its encoding gene, preparation process and application thereof
A superantigen and small molecule technology, applied in the field of genetic engineering, can solve the problems of unclear research conclusions, few structures and functions, and achieve the effects of high tumor inhibitory activity, low serum reactivity, high expression and purification
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Embodiment 1
[0031] 1) Small molecular superantigen modified body protein gene having the base sequences of SEQ ID NO: 1, SEQ ID NO: 3 and SEQ ID NO: 5 in the sequence table:
[0032] Small molecule superantigen modified body protein gene with sequence table SEQ ID NO: 1 base sequence:
[0033] 001 tcaagtgagt ttactggtac gatgggtaat atgaaatatt tatatgatga
[0034] 051 tcattatgta tcagcaacta aagttatgtc tgtagataaa tttttggcac
[0035] 101 atgatttaat ttataacatt agtgataaaa aactaaaaaa ttatgacaaa
[0036] 151 gtgaaaacag agtttattaaa tgaagatta gcaaagaagt acaaagatga
[0037] 201 agtagttgat gtgtatggat caaattacta tgtaaactgc tatttttcat
[0038] 251 ccaaagataa tgtaggtaaa gttacaggtg gtaaaacttg tatgtatgga
[0039] 301 ggaataacaa aacatgaagg aaaccacttt gataatggga acttataa
[0040] Information on SEQ ID NO.1 (see Sequence Listing)
[0041] (a) Sequence features:
[0042] * Length: 348 bp
[0043] *Type: nucleic acid
[0044] * Chain type: double chain
[0045] *Topology: Linear
[0046] (b) Molecular ty...
Embodiment 2
[0161] Embodiment 2 PCR amplification of small molecule superantigen recombinant protein gene
[0162] 1) Extraction of Staphylococcus aureus genomic DNA
[0163] A single colony of Staphylococcus aureus was inoculated into 5 ml of liquid LB medium, cultured on a shaker at 37°C overnight, and 1.5 ml of the culture was collected by centrifugation. Extraction of Staphylococcus aureus genomic DNA (the genomic DNA extraction procedure was performed according to F. Osber, R. Brent, R.E. Kingston, D.D. Moore, J.G. Seidman, J.A. Smith, K. Stall "Essential" Compilation of Molecular Biology Experiment Guide, New York John Wiley & Sons Publishing House, 1995 Third Edition P39-40).
[0164] 2) PCR primer design and reaction conditions:
[0165] Use the primer design software Primer5.0 to design the end primers shown below and the mutation primers shown in Table 1:
[0166] F2: 5'-CGGAATTCGAGAGTCAACCAGA-3'
[0167] R2: 5'-TCGCTCGAGTTATCCATCTTTGTTG-3'
[0168] The primers used were sy...
Embodiment 3
[0180] Expression of Small Molecule Superantigen Modified Protein
[0181] 1) Construction of the protein expression vector encoding the protein gene of the small molecule superantigen transformant: The gene cloning vectors pET-28a-sag1, pET-28a-sag2 and pET-28a-sag3 plasmid DNA were digested with EcoRI and XhoI, respectively. The gel recovery kit recovers the small molecule superantigen recombinant protein genes in the sequence listing SEQ ID NO: 1, SEQ ID NO: 3 and SEQ ID NO: 5. T4 DNA ligase was used to ligate into the pET-28a expression vector digested by the same double enzyme, and the expression vectors pET-28a-sag 1, pET-28a-sag2 and pET-28a-sag3 were constructed. E. coli BL21 (DE3) competent cells were transformed, and the correct recombinant clones were identified by Sanger dideoxy end termination sequencing.
[0182] 2) Induction, expression and purification of small molecule superantigen recombinant protein: inoculate a single colony of BL21(DE3) transformed with t...
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