Enterotoxin C2 superantigen mutant proteins, and coding gene and preparation and application thereof
A technology for mutating proteins and encoding genes, which is applied in the fields of application, genetic engineering, plant gene improvement, etc. It can solve the problems of limited clinical application prospects, limited clinical application and treatment, and reduced tumor inhibitory activity, achieving high-efficiency expression and purification, Meet industrial production and reduce the effect of vomiting
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Embodiment 1
[0033] Enterotoxin C2 superantigen mutant protein gene sequence with medicinal prospects having the base sequences of SEQ ID NO: 1, SEQ ID NO: 3, and SEQ ID NO: 5 in the sequence list; having the bases in SEQ ID NO: 7 in the sequence list The sec2m mutant gene sequence of the sequence; the enterotoxin C2 superantigen mutant protein sequence with medicinal prospects (see the sequence listing) having the sequence listing SEQ ID NO: 2, SEQ ID NO: 4, and SEQ ID NO: 6 amino acid sequences:
[0034] A kind of enterotoxin C2 superantigen mutant protein gene with medical prospect having the base sequence of SEQ ID NO: 1
[0035] 001 gagagtcaac cagaccctac gccagatgag ttgcacaaat caagtgagtt
[0036] 051 tactggtttg atggaaaata tgaaatattt atatgatgat cattatgtat
[0037] 101 cagcaactaa agttatgtct gtagataaat ttttggcaca tgatttaatt
[0038] 151 tataacatta gtgataaaaa actaaaaaat tatgacaaag tgaaaacaga
[0039] 201 gttattaaat gaagatttag caaagaagta caaagatgaa gtagttgatg
[0040] 251 tgtatggatc aaa...
Embodiment 2
[0184] Preparation method of enterotoxin C2 superantigen mutant protein with medicinal prospect:
[0185] ① Extraction of Staphylococcus aureus genomic DNA
[0186] Inoculate a single colony of Staphylococcus aureus in 5ml of liquid LB medium, culture overnight on a shaker at 37°C, and collect 1.5ml of the culture by centrifugation to collect the bacteria. Extract Staphylococcus aureus genomic DNA (genome DNA extraction operation presses F. Osper, R. Brent, R.E. Kingston, D.D. Moore, J.G. Seidman, J.A. Smith, K. Stellar "fine Compilation of Molecular Biology Experiment Guide, New York John Wiley & Sons Publishing House, 1995, third edition, P39-40).
[0187] ②PCR primer design and reaction conditions:
[0188] The sequences of PCR primers were designed and synthesized as follows:
[0189] sec2-F: 5'-CGG AAT TCG AGA GTC AAC CAG A-3'
[0190] sec2-R: 5'-TCG CTC GAG TTA TCC ATT CTT TGT TG-3'
[0191] F-Mutant, 5'-GTT TAC TGG TTT GAT GGA AAA TAT GAA ATA T-3'
[0192] R-Mutan...
Embodiment 3
[0216] Superantigen Activity Detection
[0217] The SPF-grade pure-line mouse Balb / c was sacrificed through the cervical spine, and the spleen was collected under aseptic conditions, crushed lightly, and passed through a 200-mesh sieve. Then the cell suspension passed through the sieve was centrifuged at 1000rpm / min for 5min to collect the cell pellet, the cells were resuspended with 5mL red blood cell lysate, left to stand for 5min and then centrifuged at 1000rpm / min for 5min. Then wash the cells 1-2 times with serum-free 1640 medium (purchased from Gibco), and finally adjust the cell concentration with RPMI-1640 medium containing 10% calf serum (purchased from Gibco) to 8×10 5 cells / well added to 96-well plate. Each purified mutein was added to each well at a final concentration of 10 ng / ml, 100 ng / ml, 1000 ng / ml, and 10000 ng / ml. BSA was used as a negative control, and SEC2 standard was used as a positive control, and three replicate wells were set up for each concentrati...
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