Anti-Inflammatory Antibodies Target Complement Inhibitors
A technology of inhibitors and complement, applied in the field of gene products, can solve problems such as infection
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Embodiment 1
[0058] Example 1. Acquisition of anti-P-selectin single-chain antibody targeting complement inhibitor ScFv-CD59 and construction of its eukaryotic expression vector
[0059] 1. Obtaining anti-P-selectin single chain antibody
[0060] Use the following method to screen anti-P-selectin single-chain antibody, and the specific method includes the following steps:
[0061] 1. Cell culture and identification: the hybridoma cells secreting P-selectin antibody (constructed with reference to the hybridoma cell and monoclonal antibody experimental technology, Xu Tinggui, 1982.) were cultured in complete RPMI1640 medium containing 15% bovine serum middle. Incubator with 5% CO 2 A mixed gas with a humidity of 98%. The specificity and titer of the monoclonal antibody in the culture supernatant were identified by ELISA method, and the antibody titer reached 1:3200 with obvious species specificity. .
[0062] 2. Isolation and purification of mRNA: use rapid preparation and purification ...
Embodiment 2
[0077] Example 2. Screening of cell lines with high expression of anti-P-selectin single-chain antibody targeting complement inhibitor ScFv-CD59 and purification of anti-P-selectin single-chain antibody targeting complement inhibitor ScFv-CD59
[0078] 1. Screening of cell lines with high expression of anti-P-selectin single chain antibody targeting complement inhibitor ScFv-CD59
[0079] In order to obtain higher biological protein molecules that are closer to natural proteins in terms of molecular structure, physical and chemical properties and biological functions, the recombinant eukaryotic expression plasmid pEE14.1 / ScFv-CD59 obtained in Example 1 was transfected into Chinese hamsters using liposomes Ovarian cells in CHO. After 24 hours of transfection, the medium was sucked off, and 10 mL of fresh selective medium DMEM+10% FCS+25 μm MSX was added. at 5% CO 2 The mixed gas was cultivated in a 37°C incubator with a humidity of 98%. After 2 weeks, clones of about 1-2 mm ...
Embodiment 3
[0082] Embodiment 3, in vivo and in vitro biological activity identification and animal experiments
[0083] 1. Complement lysis inhibition experiment
[0084] To measure the inhibitory activity on complement, 60%-80% confluent CHO cells were separated with ethylenediaminetetraacetic acid, washed twice with DMEM, and then resuspended in DMEM to make the final concentration of 10 9 / L. Add 100mL / L rabbit anti-CHO cell membrane antiserum to the cell suspension and react at 4°C for 30min to sensitize the cells. Then the antiserum was discarded, and the cells were resuspended in NHS diluted with DMEM to a final volume of 50 μl or 100 μl. After 60 minutes at 37°C, the cell viability was measured by placenta blue staining and exclusion method (both live and dead cells were counted). The fusion protein ScFv-CD59 was diluted with DEME and added to NHS first, and then added to CHO cell suspension. The final concentration was based on the control CHO cells lysed by 100 g / L NHS which...
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