insulin-fc fusion protein
A technology of fusion protein and insulin, which is applied in the field of its preparation and fusion protein, can solve the problems of inconvenient transportation and storage, inability to cure diseases, and short half-life of storage, etc., to improve pharmacokinetic performance, reduce medication pain, and reduce intervals the effect of time
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Embodiment 1
[0023] Example 1: Construction and expression of insulin-Fc fusion protein
[0024] Lymphocytes from healthy people were separated with lymphocyte separation fluid, and total RNA was extracted with Trizol reagent (product of Invitrogen Company), according to the literature (Cell, 1980, 22: 197-207) and literature (NucleicAcidsResearch, 1982, 10: 4071-4079) reports Primers FCMSENSE: GAGCCCAAATCTTGTGACAAAACTCACACATGCCCACCGTGCCCAGCACCTGAAGCAGCAGGGGGACCGTCAGTCTTCC and FCANTISENSE: CGAATTCTCATTTACCCGGAGACAGG were designed to amplify the Fc region of the antibody, and mutation points were introduced into FCMSENSE to mutate the two leucines of H235 and H236 into two alanines. All the reactions were hot-started, and the reaction conditions were: 94°C for 5 minutes; 94°C for 45 seconds, 60°C for 45 seconds, 72°C for 1 minute and 10 seconds, 30 cycles; 72°C for 10 minutes. Insulin B chain, C is 1, GGGPGKR, 2, GGGPQT, 3, GGGPGAG, 4, AAGGGPSVR) and A chain genes were synthesized from the ...
Embodiment 2
[0026] Example 2: Detection of insulin-Fc fusion protein affinity
[0027] ELISA identifies the binding activity of insulin-Fc fusion protein: the soluble insulin receptor protein (Abnova company product) is diluted to 2ug / ml with 0.05mmol / L sodium carbonate.Sodium bicarbonate buffer (pH9.6), 100ul / well, Coating overnight at 4°C. After blocking with 3% skimmed milk at room temperature for 2 hours, different concentrations of insulin-Fc fusion protein and control antibody 301 were added, 100ul / well, and 3 parallel wells were taken for each concentration, and incubated at room temperature for 2 hours. Discard the supernatant, wash with PBS three times, add HRP-labeled mouse anti-human IgG monoclonal antibody (product of DAKO Company) diluted according to the titer, 50 μl / well, and incubate at room temperature for 45 minutes. After fully washed with PBS, the OPD was protected from light for color development, and 2mol / L H2SO4 was added to terminate the reaction, and the absorban...
Embodiment 3
[0029] Embodiment 3: Detection of the affinity constant of insulin-Fc fusion protein with biocore
[0030] BiacoreT100 was used to detect the binding activity of each insulin-Fc fusion protein to insulin receptor. The insulin receptor was connected to the CM5 chip by the amino coupling method, and then the insulin receptor and each insulin-Fc were analyzed in Biacore universal buffer (10mM Hepes pH 7.4, 150mM NaCl, 3mM EDTA, 0.005% surfactantP-20) according to the operating instructions. For the binding activity of the fusion protein, the flow rate of the flow cell was 30ul / min. The insulin receptor is coupled to a response value of 1500RU, and insulin and each insulin-Fc fusion protein (50ug / ml, 25ug / ml, 12.5ug / ml, 6.25ug / ml, 3.125ug / ml, 1.56ug / ml, 0.78ug / ml, 0.39ug / ml) the signal activity of interacting with the insulin receptor at different concentrations. The binding time was 420 s, the dissociation time was 600 s, and the regeneration time was 60 s with 10 mM glycine. T...
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