Expression and identification of the HCV core protein in the human hepatocyte QSG7701
Li Jun
Abstract
Li Jun
Abstract
Objective:To construct a recombinant plasmid enconding HCV core gene and induce the expression of core protein in the human hepatocyte and identify the core protein.Methods:HCV core gene was clone by using PCR from plasmid pBRTM/HCV1-3011 which concludes the full length of HCV gene.We recombined the core segment with expression plasmid pcDNA3.1(-) to construct eukaryotic plasmid pcDNA3.1(-)/core.Then the plasmid pcDNA3.1(-)/core was transfected into human hepatocytes by using poly-cation.The expression of core protein was detected by immunochemical staining method and Western blot.Results:The clone core segment had correct length and sequence the QSG7701 cells were successfully transfected and expressed core protein.Conclusion:We have successfully constructed eukaryotic expression plasmid pcDNA3.1(-)/core which included the HCV core gene.And the vector successfully expressed core protein in human hepatocytes these result provide a good core protein expression system for the study of the hepatocarcinogesis of the core protein and lay foundation for developing the HCV DNA vaccine.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective:To construct a recombinant plasmid enconding HCV core gene and induce the expression of core protein in the human hepatocyte and identify the core protein.Methods:HCV core gene was clone by using PCR from plasmid pBRTM/HCV1-3011 which concludes the full length of HCV gene.We recombined the core segment with expression plasmid pcDNA3.1(-) to construct eukaryotic plasmid pcDNA3.1(-)/core.Then the plasmid pcDNA3.1(-)/core was transfected into human hepatocytes by using poly-cation.The expression of core protein was detected by immunochemical staining method and Western blot.Results:The clone core segment had correct length and sequence the QSG7701 cells were successfully transfected and expressed core protein.Conclusion:We have successfully constructed eukaryotic expression plasmid pcDNA3.1(-)/core which included the HCV core gene.And the vector successfully expressed core protein in human hepatocytes these result provide a good core protein expression system for the study of the hepatocarcinogesis of the core protein and lay foundation for developing the HCV DNA vaccine.
Key concepts: Plasmid, Molecular biology, Transfection, clone (Java method), Recombinant DNA, Gene, Biology, Expression vector