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Objective To study the mechanism of the cellular proteins involved in the process of replication of hepatitis C virus (HCV) negative-strand RNA.Methods Ultraviolet (UV) cross-linking was used to identify the cellular proteins that would bind to the 3’ -end of HCV negative-strand RNA. Competition experiment was used to confirm the specificity of this binding, in which excess nonhomologous protein and RNA transcripts were used as competitors. The required binding sequence was determined by mapping, then the binding site was predicted through secondary structure analysis.Results A cellular protein of 45 kD (p45) was found to bind specifically to the 3’ -end of HCV negative-strand RNA by UV cross-linking, nhomologous proteins and RNA transcripts could not compete out this binding, whereas the unlabeled 3’ -end of HCV negative-strand RNA could. Mapping of the protein-binding site suggested that the 3’ -end 131-278nt of HCV negative-strand RNA was the possible protein-binding region. Analysis of RNA secondary
Objective To study the mechanism of the cellular proteins involved in the process of replication of hepatitis C virus (HCV) negative-strand RNA. Methods Ultraviolet (UV) cross-linking was used to identify the cellular proteins that would bind to the 3 ’ end of HCV negative-strand RNA. Competition experiment was used to confirm the specificity of this binding, in which excess nonhomologous protein and RNA transcripts were used competitors. The required binding sequence was determined by mapping, then the binding site was predicted through secondary structure analysis. Results A cellular protein of 45 kD (p45) was found to bind specifically to the 3 ’-end of HCV negative-strand RNA by UV cross-linking, nhomologous proteins and RNA transcripts could not compete out this binding, unlabeled 3 ’-end of HCV negative-strand RNA could. Mapping of the protein-binding site suggested that the 3’ -end 131-278nt of HCV negative-strand RNA was the possible protein-binding region. Analysi s of RNA secondary