Anti-IL5 nano antibody and application thereof
A nanobody, antibody technology, applied in the field of biomedicine or biopharmaceuticals
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Embodiment 1
[0226] Example 1: Screening of IL5-specific Nanobodies by Phage Display Technology
[0227] In the early stage, high-purity human IL5 protein was mixed with immune adjuvant, and 2 Xinjiang Bactrian camels were immunized. After 7 times of immunization, peripheral blood was collected, and then lymphocytes were extracted from it to isolate RNA. After reverse transcription of the RNA, the VHH gene was isolated by nested PCR amplification, and then the VHH fragment was cloned into the pMECS vector, and then electrotransformed into TG1 competent cells to establish an anti-IL5 nanobody phage display library. It was determined that the storage capacities of the two libraries were 6.4×10 8 CFU and 1.3×10 8 The insertion rates of CFU and VHH of the target fragment of the library were 91.7% and 100%, respectively. Then, phage display technology was used to screen IL5-specific Nanobodies. For the specific screening method, refer to the scheme in Example 3 of patent CN110144011B. After ...
Embodiment 2
[0228] Example 2: Blocking IL5 Nanobody Screening
[0229] Inoculate IL5 nanobody clones with different sequences in 1 mL of TB medium containing appropriate concentration of ampicillin, and culture on a constant temperature shaker at 37°C until logarithmic growth phase, add IPTG inducer, induce at 28°C for 16h; after 16h, use osmotic Shred the bacteria by pressure shock method to obtain the crude nanobody extract; take 1E6 HEK293F / IL5Ra cells from each sample and resuspend in 0.5% BSA-PBS buffer, add 200 μL of the above IL5 nanobody crude extract, and set a negative control at the same time (lysate), add appropriate concentration of IL5-Biotin to all samples, incubate at 4°C for 20 minutes; wash twice with 1×PBS, add SA-PE, incubate at 4°C in the dark for 20 minutes, wash cells twice with PBS and use Flow cytometry (BD Caliber) detection, the results are as follows figure 2 Shown: 11 strains of IL5 nanobodies with good blocking effect were preliminarily screened, and the lo...
Embodiment 3
[0233] Example 3: Species-specific detection of IL5 Nanobodies
[0234] ELISA was used to detect whether the 11 strains of Nanobodies obtained in Example 2 could cross-react with IL5 from other species. Add 1 μg / mL human IL5, mouse IL5, cynomolgus IL5 and IgG1 proteins to the microtiter plate and coat overnight, 4°C, 100uL / well; after washing 5 times with PBST, add 300uL 1% BSA to each well at room temperature Block for 2 hours; after washing 5 times with PBST, add 100uL 2μg / mL prokaryotic expressed Nanobodies (Nb6, Nb13, Nb20, Nb21, Nb25, Nb26, Nb50, Nb66, Nb71, Nb85, Nb92) and incubate at 37°C 1 hour; wash 5 times with PBST, add 100uL diluted mouse anti-HA antibody (diluted 1:2000) and incubate at 37°C for 1 hour; wash 5 times with PBST, add 100uL diluted alkaline phosphatase modified anti-mouse Antibody (diluted at 1:2000) was incubated at 37°C for 1 hour; then washed 5 times with PBST, added with chromogenic solution, and the absorbance was measured with a microplate read...
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