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Updated: Aug 24, 2026

A Protocol for Analyzing Hepatitis C Virus Replication
Published on: June 26, 2014
Expression and purification of untagged full-length HCV NS5B RNA-dependent RNA polymerase
Q May Wang1, Robert B Johnson, Dayue Chen
1Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN 46285, USA. qmwang@lilly.com
Abstract:
The NS5B encoded by the hepatitis C virus genome is a RNA-dependent RNA polymerase essential to viral replication. The entire NS5B protein contains a catalytic domain followed by a regulatory motif and a membrane-anchor domain at its C-terminus. Reported here is the molecular cloning and expression of the full-length NS5B polymerase (NS5B-FL) in bacterial cells as a non-fusion protein. The non-tagged NS5B-FL was purified to homogeneity using sequential chromatographic columns and its identity was confirmed using anti-NS5B peptide antibodies and amino acid sequencing. Purified NS5B-FL demonstrated RNA-dependent RNA polymerase activity and was able to replicate a HCV RNA genome fragment through both copy-back and de novo mechanisms. Its biochemical properties were further characterized in comparison with a truncated form of NS5B polymerase with a deletion of 51 residues from its C-terminus.

