Hepatitis C Virus E2 외피항원에 대한 단일클론항체의 특성 연구

Characterization of Monoclonal Antibody Specific for Hepatitis C Virus E2 Envelope Protein

  • 박준상 (목암 생명공학 연구소 고등생물유전자 발현실) ;
  • 이범용 (목암 생명공학 연구소 고등생물유전자 발현실) ;
  • 정수일 (목암 생명공학 연구소 고등생물유전자 발현실) ;
  • 민미경 (목암 생명공학 연구소 고등생물유전자 발현실)
  • Park, Joon-Sang (Eukaryotic Gene Expression Lab, Mogam Biotechnology Research Institute) ;
  • Lee, Bum-Young (Eukaryotic Gene Expression Lab, Mogam Biotechnology Research Institute) ;
  • Chung, Soo-Il (Eukaryotic Gene Expression Lab, Mogam Biotechnology Research Institute) ;
  • Min, Mi-Kyung (Eukaryotic Gene Expression Lab, Mogam Biotechnology Research Institute)
  • 발행 : 1997.06.30

초록

Hepatitis C virus (HCV) E2 protein is known to be one of putative envelope proteins. To develop a sensitive detection method for HCV infected tissues and cells, monoclonal antibodys (MAbs) to the E2 protein of HCV were prepared from mice immunized with recombinant baculovirus-expressing E2 protein (Bac-E2). Several hybridoma clones secreting various levels of MAb were isolated and isotypes of these MAb were determined. One clone (L.2.3.3) was used for ascites production and the E2-MAb was purified and characterized. The L.2.3.3 reacted well with both Bac-E2 and E. coli expressed glutathione-S-transferase-E2 (GST-E2) fusion proteins. Using HCV patient sera, E2 envelope protein was found to be localized in the cell membrane boundary both in CHO cells and insect cells which express HCV E2 protein. Similar result was obtained when same cells were treated with the MAb L.2.3.3. These results demonstrated that Bac-E2 protein is capable of eliciting high titer antibody production in mice.

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