| Literature DB >> 34395740 |
Jin-Wei Zheng1, Jia-Li Cao2, Quan Yuan2.
Abstract
The stable HBV-transfected cell lines, which based on stable integration of replication-competent HBV genome into hepatic cells, are widely used in basic research and antiviral drug evaluation against HBV. However, previous reported strategies to generate HBV-replicating cell lines, which primarily rely on random integration of exogenous DNA by plasmid transfection, are inefficient and time-consuming. We newly developed an all-in-one Sleeping Beauty transposon system (denoted pTSMP-HBV vector) for robust generation of stable HBV-replicating cell lines of different genotype. The pTSMP-HBV vector contains HBV 1.3-copy genome and dual selection markers (mCherry and puromycin resistance gene), allowing rapid enrichment of stably-transfected cells via red fluorescence-activated cell sorting and puromycin antibiotic selection. In this protocol, we described the detailed procedure for constructing the HBV-replicating stable cells and systematically evaluating HBV replication and viral protein expression profiles of these cells.Entities:
Keywords: HBV; HBV 1.3-copy genome; HBV-replicating cell lines; HepG2; Sleeping Beauty transposon system
Year: 2018 PMID: 34395740 PMCID: PMC8328597 DOI: 10.21769/BioProtoc.2908
Source DB: PubMed Journal: Bio Protoc ISSN: 2331-8325