Polypeptide sequence specifically binding to porcine circovirus type 2 cap protein and its application
A porcine circovirus, specific technology, applied in the direction of virus peptides, peptides, peptide sources, etc., can solve the problems of economic losses in the pig industry, and achieve the effects of rapid artificial synthesis, good specificity, and low detection costs
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Embodiment 1
[0022] Example 1 Molecular docking and screening of virtual peptide library
[0023] 1. Preparation of Cap protein crystal structure
[0024] The amino acid sequence and crystal structure of porcine circovirus type 2 Cap protein were analyzed with the help of computer-aided design software, and the 63rd to 120th amino acid residues were selected as the docking region for molecular docking.
[0025] 2. Design of virtual peptide library
[0026] The present invention adopts the method of extending amino acid residues one by one. First, several amino acid libraries with the highest scores are docked with the structure of the target protein one by one. Until the best docking result is achieved. The peptide sequence generated by the virtual peptide library preferably has 2-9 amino acid residues.
[0027] 3. Evaluation of docking results
[0028] Separately calculate the free energy of peptide-protein binding, hydrogen chain, van der Waals force and other mechanical parameters f...
Embodiment 2
[0029] Example 2 Affinity Identification of L6-11 Sequence and Artificially Expressed Cap Protein
[0030] 1. The first is the preparation of the Cap protein chip, using the EDC / NHS method to covalently couple the PCV2Cap protein (5 μg / mL) to the carboxyl chip of LSPR. When the LSPR Single≥500pm, it indicates that Cap protein coupling is successful, and this sensor can be used to measure the interaction between PCV2Cap protein and L6-11 sequence.
[0031] 2. The second is to run the sensor to obtain a stable signal baseline. Start running PBS buffer (pH 7.4) at the highest flow rate of 150 μL / min until the signal baseline of the sensor reaches a stable level. Then, reduce the flow rate to 20 μL / min and prepare for loading. Sample.
[0032] 3. Use PBS buffer to pre-preparate the dry powder of L6-11 synthesized in solid phase and modified by biotinylation at the amino terminal to different concentrations, and then inject 300 μL of L6-11 solutions of different concentrations int...
Embodiment 3
[0034] Example 3 ELISA Identification of L6-11 Sequence and Artificially Expressed Cap Protein
[0035] 1. Dilute the purified PCV2Cap protein with CBS solution (pH9.6) to 10 μg / mL, and add it to an ELISA 96-well plate at a volume of 50 μL / well; express the purified protein from different viruses in the same way, that is, classical swine fever virus E2 protein (CSFV-E2), porcine epidemic diarrhea virus S protein (PEDV-S) and 1% bovine serum albumin (BSA), PBS buffer for ELISA 96-well plate coating, as a control, overnight coating at 4 °C .
[0036] 2. The ELISA plate was washed 5 times with PBST buffer, and incubated with 1% BSA solution at 37°C for 1 hour.
[0037] 3. Use PBS buffer to dilute the solid-phase synthesized L6-11 polypeptide to a working concentration of 1 μg / mL, add it to the above ELISA plate at a volume of 50 μL / well and mix well, wash the ELISA plate with PBST buffer at 37°C for 30 minutes 5 times.
[0038] 4. Dilute horseradish peroxidase-labeled avidin (...
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