Avian metapneumovirus (aMPV) F protein polypeptide and application thereof
A technology of protein polypeptide and carrier protein, which is applied in the direction of antiviral immunoglobulin, peptide, hybrid peptide, etc., can solve the problems that have not been reported, and achieve the effect of high sensitivity, high conservatism, and stable sensitivity
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Embodiment 1
[0028] The determination of embodiment 1 avian metapneumovirus F protein antigen short peptide
[0029] According to the protein sequence of the F gene of avian metapneumovirus, bioinformatics analysis and comparison were carried out to determine the following polypeptide: CTNAGSTAYYPNKDD was named as the F protein polypeptide as the short antigenic peptide. The antigen short peptide has high conservation and strong antigenicity, and was synthesized by Shanghai Jier Biochemical Company. The coupling is based on the maleimide theory, that is, the cysteine residue in the polypeptide sequence and the amino group in the carrier protein coupling. Therefore, when designing a polypeptide antigen, a cysteine residue is often added to its N-terminal or C-terminal to facilitate the coupling of the polypeptide to the carrier protein.
Embodiment 2
[0030] The preparation of embodiment 2 monoclonal antibody
[0031] 1) Peptide conjugation and animal immunization
[0032] Peptides were conjugated to KLH (Pierce Cat#77611) and BSA (AMRESCO code0332). After desalting, the KLH-coupled peptide was mixed with an equal amount of CFA or IFA as an immunogen and stored at 4 degrees. Three BALB / c mice were immunized with the immunogen mixed with CFA on day 0, and then boosted with the immunogen mixed with IFA several times in the following days. On the 14th day, the tail blood of the mice was drawn, coated with uncoupled polypeptide and carrier protein BSA-coupled polypeptide, and the corresponding titers were detected by ELISA to observe the immune response against the antigen.
[0033] The detection method of ELISA is: add 100ng detection original to each well of 96-well plate (Corning, USA), wrap the plate overnight at 4°C. After washing twice with phosphate buffered saline (PBS), block with 5% skimmed milk powder PBS for one ...
Embodiment 3
[0060] Example 3 The IFA method and immunoblotting (WB) method of monoclonal antibody preparation are used for the detection of avian metapneumovirus infection
[0061] The monoclonal antibody produced by the monoclonal antibody strain 2B8 was used to detect the infection of avian metapneumovirus on Vero cells, using indirect immunofluorescence (IFA) and immunoblotting (WB) methods for detection. The IFA detection method is as follows: Vero cells grown into a single layer in a 96-well cell plate were washed twice with phosphate buffered saline (PBS), then inoculated with avian metapneumovirus, and cultured at 37°C in an incubator containing 5% CO2; At a given time point after virus inoculation, fix with 4% paraformaldehyde at room temperature for 30 minutes; after washing, the cell wells were washed with 1:30 times diluted anti-Avian metapneumovirus F protein monoclonal antibody (the dilution solution is 3%BSA- PBS) at 37°C for 90 minutes; after washing, the cell wells were in...
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