2012PubMedRequires access

[Preparation and identification of monoclonal antibodies against recombinant N protein of mouse hepatitis virus].

Jie Zhou, Li Zhao, Jianhua Hu, Cheng Gao

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Abstract

AIM: To prepare and characterize the monoclonal antibodies (mAbs) against N protein of mouse hepatitis virus (MHV). METHODS: BALB/c mice were immunostimulated with the purified recombinant N protein expressed by Bac-to-Bac baculovirus expression system. Then the spleen cells of the immunized mice were fused with Sp2/0 myeloma cells by conventional hybridoma techniques. An indirect ELISA using recombinant N protein as antigen was established to screen antibody-producing hybridoma cell lines. Western blotting and IFA were applied to characterize the mAbs. RESULTS: We obtained four hybridoma cell lines secreting mAbs against recombinant N protein. The subclasses of two mAbs were IgG2a, one IgG2b and the other IgG1, and light chains were both Kappa. Western blotting showed that the mAbs specifically recognized certain antigenic epitope of N protein of MHV. CONCLUSION: mAbs against N protein of MHV with high activity and specificity were prepared successfully, which provides a potential basis for further researches on N protein function and diagnostic methods.

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What this paper is about

AIM: To prepare and characterize the monoclonal antibodies (mAbs) against N protein of mouse hepatitis virus (MHV). METHODS: BALB/c mice were immunostimulated with the purified recombinant N protein expressed by Bac-to-Bac baculovirus expression system. Then the spleen cells of the immunized mice were fused with Sp2/0 myeloma cells by conventional hybridoma techniques. An indirect ELISA using recombinant N protein as antigen was established to screen antibody-producing hybridoma cell lines. Western blotting and IFA were applied to characterize the mAbs. RESULTS: We obtained four hybridoma cell lines secreting mAbs against recombinant N protein. The subclasses of two mAbs were IgG2a, one IgG2b and the other IgG1, and light chains were both Kappa. Western blotting showed that the mAbs specifically recognized certain antigenic epitope of N protein of MHV. CONCLUSION: mAbs against N protein of MHV with high activity and specificity were prepared successfully, which provides a potential basis for further researches on N protein function and diagnostic methods.

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Available abstract

AIM: To prepare and characterize the monoclonal antibodies (mAbs) against N protein of mouse hepatitis virus (MHV). METHODS: BALB/c mice were immunostimulated with the purified recombinant N protein expressed by Bac-to-Bac baculovirus expression system. Then the spleen cells of the immunized mice were fused with Sp2/0 myeloma cells by conventional hybridoma techniques. An indirect ELISA using recombinant N protein as antigen was established to screen antibody-producing hybridoma cell lines. Western blotting and IFA were applied to characterize the mAbs. RESULTS: We obtained four hybridoma cell lines secreting mAbs against recombinant N protein. The subclasses of two mAbs were IgG2a, one IgG2b and the other IgG1, and light chains were both Kappa. Western blotting showed that the mAbs specifically recognized certain antigenic epitope of N protein of MHV. CONCLUSION: mAbs against N protein of MHV with high activity and specificity were prepared successfully, which provides a potential basis for further researches on N protein function and diagnostic methods.

Key concepts: Monoclonal antibody, Recombinant DNA, Molecular biology, Epitope, Virology, Antibody, Blot, Antigen

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