Abstract
Hepatitis C virus (HCV) F protein is a newly discovered HCV gene product that is expressed by translational ribosomal frameshift. Little is known about the biological properties of this protein. By performing pulse-chase labeling experiments, we demonstrate here that the F protein is a labile protein with a half-life of < 10 min in Huh7 hepatoma cells and in vitro. The half-life of the F protein could be substantially increased by proteasome inhibitors, suggesting that the rapid degradation of the F protein is mediated by the proteasome pathway. Further immunofluorescence staining and subcellular fractionation experiments indicate that the F protein is primarily associated with the endoplasmic reticulum. This subcellular localization is similar to those of HCV core and NSSA proteins, raising the possibility that the F protein may participate in HCV morphogenesis or replication.
Original language | English (US) |
---|---|
Pages (from-to) | 1578-1583 |
Number of pages | 6 |
Journal | Journal of virology |
Volume | 77 |
Issue number | 2 |
DOIs | |
State | Published - Jan 2003 |
Externally published | Yes |
ASJC Scopus subject areas
- Insect Science
- Virology
- Microbiology
- Immunology