Interferon mutant and interferon mutant fusion antibody and its preparation method and application
A technology for fusing antibodies and mutants, applied in the field of bioengineering, can solve the problems of short half-life of interferon and strong systemic side effects
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Embodiment 1
[0037] Example 1 Construction of the recombinant plasmid of anti-VEGFR2-IFNαmut
[0038] According to the existing anti-VEGFR2 fusion antibody anti-VEGFR2-IFNα (refer to literature Li Z, Zhu Y, Li C, et al. Anti-VEGFR2-interferon-α2 regulates the tumor microenvironment and exhibits potent antitumor efficacy against colorectal cancer[J].Oncoimmunology , 2017,6(3):e1290038.doi:10.1080 / 2162402X.2017.1290038.) to prepare a recombinant plasmid for constructing anti-VEGFR2-IFNαmut; the anti-VEGFR2-IFNα is coupled at the C-terminus of the Fc segment of the antibody through G4S Linker For the fusion antibody linked with IFNα, in its heavy chain expression plasmid, the two ends of the part expressing IFNα contain restriction sites BamHI and PmeI. Based on this, we first obtained the expression sequence of IFNα by double enzyme digestion of the plasmid, and then, using IFNα as a template, designed mutation primers, obtained IFNαmut by overlapping PCR, and then based on the obtained IFNα...
Embodiment 2
[0061] Example 2 Expression, purification and SDS identification of anti-VEGFR2-IFNαmut
[0062] The light and heavy chains were transiently transfected into CHO cells, and stable and high-yielding monoclonal cell lines were selected by pressure selection and two limited dilution methods. The stable high-yielding cell line was expanded and cultivated, the supernatant was collected, centrifuged at 6000rpm, 4°C for 30min, filtered with a 0.22μm filter membrane, purified with a Protein A affinity chromatography column, and the eluent was used to elute the protein. The purified anti-VEGFR2-IFNαmut and anti-VEGFR2-IFNα were mixed with non-reduced SDS-PAGE loading buffer at a ratio of 4:1 (20μl:5μl) in an Eppendorf tube, placed in a water bath at 100°C for 5 minutes and then 3000rpm After centrifugation for 5 minutes, the protein sample was ready for use. Configure 10% SDS-PAGE gel for electrophoresis, stop electrophoresis after 80mA constant current for 30min, 120min constant curr...
Embodiment 3
[0063] Example 3 Western Blot identification of anti-VEGFR2-IFNαmut
[0064] The purified anti-VEGFR2-IFNαmut and anti-VEGFR2-IFNα were subjected to SDS-PAGE electrophoresis, 80V constant voltage for 30min, 120V constant voltage for 30min, transfer for 2h, and the protein was transferred to PVDF membrane (purchased from Millipore); the transfer was completed , block the membrane in 5% MTBS (TBS containing 5% skimmed milk) at room temperature for 2h; dilute the primary antibody with 5% MTBS at 1:2000 (A&B picture is HRP-coupled goat anti-human Fc antibody, without Anti-antibody; C&D picture is rabbit anti-human κ chain antibody; E&F picture is mouse anti-human IFNα antibody) (purchased from abcam), incubated at room temperature for 1.5h, washed three times with TBST and three times with TBS, each time for 10min; Dilute the secondary antibody with % MTBS at 1:5000 (C&D picture is the HRP-coupled goat anti-rabbit secondary antibody; E&F picture is the goat anti-mouse secondary an...
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