Application of hepatic cell growth regulatory factor tyrosine kinase substrate in prevention and/or treatment of EV71 infection
A technology for growth regulators and tyrosine kinases, which is used in medical preparations containing active ingredients, peptide/protein ingredients, antiviral agents, etc.
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Embodiment 1
[0023] Example 1 Preparation of hepatocyte growth regulator factor tyrosine kinase substrate
[0024] (1) Cloning of the hepatocyte growth regulator tyrosine kinase substrate gene: using the total mRNA extracted from human blood leukocytes as a template, the total cDNA was first amplified by reverse transcription PCR, and then the cDNA was used as a template to use specific The primers amplified the complete HGS gene fragment. Primers are as follows:
[0025] P1 (forward primer): 5'-AA GGATCC ATGGGGCGAGGCAGCGG-3', BamHI,
[0026] P2 (reverse primer): 5'-AA CTCGAG TCAGTCGAATGAAATGA-3', XhoI.
[0027] The HGS gene was cloned under the pTAC promoter of the vector pGEX-6p-1 by restriction digestion and ligation of BamHI and XhoI to obtain the expression vector pGEX-6p-1-HGS of HGS.
[0028] (2) Acquisition of Escherichia coli expressing hepatocyte growth regulator factor tyrosine kinase substrate: the above expression vector pGEX-6p-1-HGS was transformed into Escherichia co...
Embodiment 2
[0031] Example 2 Detection of toxicity of hepatocyte growth regulator factor tyrosine kinase substrate to host cells
[0032] After 24-48 hours of culturing human malignant embryonic rhabdomyosarcoma cells (rhabdomyosarcoma, RD) grow into a single layer (MEM medium + 10% fetal bovine serum culture), discard the culture medium, add trypsin to digest, transfer to 96-well sterile In a cell culture plate, 100 μL per well, placed at 37°C, 5% CO 2 Culture in the cell incubator for 18-24h to make the cells grow into a single layer, discard the supernatant. The HGS cryopreservation solution obtained in Example 1 was diluted step by step with serum-free MEM cell culture medium, and prepared into four concentration gradients of 8, 40, 200, and 1000 μg / mL, and then added different concentrations of HGS protein solution and discarded In the cell culture wells of the supernatant, 100 μL per well, repeat 3 wells for each concentration, and set up cell control wells (without adding drugs, o...
Embodiment 3
[0036] Example 3 Anti-EV71 virus effect of hepatocyte growth regulator factor tyrosine kinase substrate
[0037] After 24-48 hours of culture, human malignant embryonic rhabdomyosarcoma cells (RD cells) grow into a single layer (MEM medium + 10% fetal bovine serum), discard the culture medium, add trypsin to digest, and transfer to 96-well sterile cells In the culture plate, 100 μL per well, placed at 37 ° C, 5% CO 2 Culture in the cell incubator for 18-24h to make the cells grow into a single layer, discard the supernatant. Add HGS protein solutions diluted with serum-free MEM cell culture medium to a final concentration of 0.6, 1.2, 2.5, 5, 10, and 20 μg / mL, and incubate for 24 hours and then infect with EV71 virus. The multiplicity of infection (MOI) The MOI was 5, and the samples were collected after 12 hours to detect the mRNA level and protein level of EV71VP1 by Realtime PCR and Western Blot respectively. Among them, Western Blot uses β-actin as an internal reference,...
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