Antigenic epitope simulative peptide of classical swine fever virus (CSFV) E2 protein, and preparation method and application thereof
A swine fever virus and peptide-mimicking technology, applied in viral peptides, biochemical equipment and methods, viruses, etc., can solve the problems of complex expression of E2 protein, and achieve process safety, short production cycle, and high sensitivity. Effect
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Embodiment 1
[0032] A preparation method of an antigenic epitope mimetic peptide of swine fever virus E2 protein, the steps are:
[0033] A. Purification and identification of E2 monoclonal antibody:
[0034] The 4A7 monoclonal antibody was purified by caprylic acid-ammonium sulfate method (Jin Boquan, Cellular and Molecular Immunology Technology. Xi'an: Fourth Military Medical University Press, 2002) (hybridoma 4A7 preservation number: CCTCC NO.C2014229, preserved in Wuhan in 2014 University China Type Culture Collection Center), and the purification effect was identified by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE). The specific steps were slightly changed, and the method was as follows: add For four parts of 0.06 mol / L (pH=5.0) acetic acid buffer solution, adjust the pH value to 4.5 with 0.1 mol / L hydrochloric acid. At room temperature (15° C. to 25° C., the same below), 3.3% octanoic acid by volume of the original ascitic fluid was slowly added, and stirred ...
Embodiment 2
[0048] A kind of analog peptide of classical swine fever virus E2 protein is used in the preparation treatment or prevention swine fever ELSIA antibody drug detection (kit), and its steps are:
[0049] A. Antigen-coated plate preparation in the swine fever ELISA antibody detection kit:
[0050] According to the 12-peptide sequence shown in SEQ ID NO: 1 of the present invention and conventional chemical synthesis methods in the art, a short peptide with a purity greater than 95% is prepared, and this short peptide is the detection antigen. Dissolve the antigen with carbonate buffer and dilute it to 2 μg / mL, then add 100 μL per well into a 96-well ELISA plate, and place it overnight at 4°C to allow the antigen to adsorb on the ELISA plate. The next day, the liquid in the wells was discarded, and 150 μL of phosphate buffered saline (containing 0.5% BSA) was added to each well, placed in a 37° C. incubator for 2 hours, and the liquid in the wells was discarded. Pat dry.
[0051]...
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