Single-chain antibody for porcine epidemic diarrhea resistant virus and application thereof
A single-chain antibody, light chain technology, applied in antiviral agents, antiviral immunoglobulins, applications, etc., can solve the problems of easy production of anti-antibodies, affecting therapeutic effects, and large molecular weight of antibodies
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Embodiment 1
[0041] Example 1, Preparation of Phage Antibody Display Library
[0042] 1. Primer design and synthesis
[0043] Primers were designed respectively according to the sequences of pig IgG heavy chain (GenBank number: AM177137, light chain Kappa chain (GenBank number: AY518084) and light chain lambda chain (GenBank number: AF345512). The nucleotide sequence and length of the amplified fragment of each primer See Table 1.
[0044] Table 1
[0045]
[0046] Note: The part in italics indicates the linker, and the underline indicates the recognition site for restriction endonuclease SfiI. The name containing "for" means upstream, the name containing "back" means downstream, VH means heavy chain, VL (Kappa) means light chain Kappa chain, VL (Lambda) means light chain lambda chain, S means C or G , Y is C or Y, K is G or T, R is A or G, W is A or T.
[0047] The respective primers shown in Table 1 were synthesized by Sangon Bioengineering (Shanghai) Co., Ltd.
[0048] 2. Extrac...
Embodiment 2
[0101] Example 2, Detection of the binding activity of the phage antibody display library
[0102] The binding activity of the phage antibody display library was detected by ELISA method.
[0103] Take porcine epidemic diarrhea virus S protein (i.e. antigen) and dilute it with pH9.6, 0.1M sodium carbonate-sodium bicarbonate buffer solution to obtain antigen dilution solution with a concentration of 100 μg / μL.
[0104] 1. Take a 96-well plate, add 100 μL of antigen diluent to each well, and leave overnight at 4°C.
[0105] 2. After completing step 1, take the 96-well plate, add 100 μL blocking solution (obtained by dissolving 0.05 g BSA in 100 mL pH7.4, 10 mM PBS buffer) to each well, and let stand at 37° C. for 2 hours.
[0106] 3. After completing step 2, take the 96-well plate, add 100 μL of phage antibody display library to each well, and let stand at 37° C. for 2 hours.
[0107] 4. After completing step 3, take the 96-well plate, add 100 μL of HRP-labeled anti-M13 antibo...
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