Recombinant interleukin 18 as well as preparation method and application thereof
A technology of interleukin and host cells, applied in the field of recombinant interleukin 18 and its preparation, can solve the problems of low renaturation rate, high price, low yield, etc., and achieve the effect of promoting activity and promoting the formation of IFN-γ
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Embodiment 1
[0098] Example 1 The prokaryotic expression vector pBV220-IL-18 of IL-18 was constructed.
[0099] The IL-18-containing gene (SEQ ID NO:2) obtained by RT-PCR was double-digested with EcoRI and BamHI, and then ligated with the vector pBV220 cut with EcoRI and BamHI; the prokaryotic expression of the IL-18-containing gene was constructed The vector pBV220-IL-18 was transformed into Escherichia coli DH5α, and the engineering strain DH5α-pBV220IL-18 was constructed; ( Figure 1~2 ).
Embodiment 2
[0100] Fermentation and high-efficiency expression of embodiment 2hrIL-18
[0101] Activation, fermentation, induction and recovery of inclusion bodies of engineered bacteria: inoculate engineered strains stored at -70°C on nutrient agar plate medium containing Amp, and culture at 37°C for more than 12 hours; pick a single colony and inoculate into LB containing Amp In the liquid medium, culture on a shaking table at 37°C for more than 12 hours; inoculate the bacterial liquid into the fermentation medium containing Amp at a ratio of 1:100, and culture on a shaking table at 32°C for more than 12 hours; inoculate the bacterial liquid into the fermentation medium at a ratio of 1:10 Cultivate in the tank at 32°C; wait until the concentration of the bacterial solution reaches OD 600 After about 2.0, the temperature was raised to 42°C to induce culture for 4 hours, and at the same time, a small amount of filler solution was continuously added, and the ammonia water automatically adj...
Embodiment 3
[0102] Refolding and purification of embodiment 3hrIL-18
[0103] 3.1 Washing, dissolution and renaturation of inclusion bodies: Weigh an appropriate amount of inclusion bodies, add inclusion body washing solution to wash twice, then add inclusion body dissolving solution at a ratio of 2%, and dissolve with magnetic stirring for more than 4 hours at 4°C; 4 ℃, 9000rpm, centrifuge for 10min, collect the supernatant; slowly add the refolding solution at a ratio of 1:8 to reduce the protein concentration to 0.2%, dissolve with magnetic stirring at room temperature for 4h; refold at 4°C for more than 20h; purify immediately.
[0104] 3.2 Purification of hrIL-18: equilibrate the hydroxyapatite chromatography column with the balance solution, load all the above-mentioned diluted refolding solution at a flow rate of 10ml / min; Elute with equilibrium solutions containing 0.1, 0.2, 0.5 and 1.0M NaCl, collect the elution peaks, and identify by SDS protein electrophoresis, the target prote...
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