Journal of Southern Medical University ›› 2004, Vol. 24 ›› Issue (01): 1-6.

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Preparation and characterization of monoclonal antibodies against S1domain at N-terminal residues 249 to 667 of SARS-associated coron-avirus S1 protein

WEN Kun1, MEI Ya-bo1, QIU Li-wen1, LIAO Zhi-yong1, Yuen Kwok-yung2, CHE Xiao-yan1   

  1. 1. 第一军医大学珠江医院中心实验室, 广东, 广州, 510282;
    2. 香港大学微生物学系, 香港
  • Online:2004-01-20 Published:2004-01-20

Abstract: Objective To prepare and characterize monoclonal antibodies (mAbs) against S1 protein of severe acute respirato-ry syndrome (SARS)-associated coronavirus (SARS-CoV).Methods 6-His-tagged recombinant fragment at N-terminal residues 249 to 667 of SARS-CoV S1 protein including S-protein receptor-binding domain was e xpressed in E.coli. The im-munogenicity of this S1 domain was identified and use d to immunize BALB/c mice for the production of hybridomas. The identification of the mAbs against this S1 domain was performed using indirect enzyme-linked im munosorbent assay (ELISA), indirect immunofluorescence assay (IFA) and Western blotting, respectively.Results Three hybridomas producing mAbs spe-cific to the S1 domain was obtained, with a relative molecular mass of 48 500. None of the 3 mAbs were reactive with human coronaviruses 229E and OC43. Two of the mAbs wer e IgG2a isotype, and the other was IgG1.Conclusion This is the first re-port of mAbs produced against S-protein receptor-binding domain of SARS-CoV. The 3 S1-s pecific mAbs may be useful for further study of the function of the S protein a nd for diagnosis of SARS-CoV infection.