Abstract
Hepatitis C virus (HCV) is a positive‐strand RNA virus that replicates its genome in a membrane‐associated replication complex. Nonstructural protein 4B (NS4B) induces the specific membrane alteration, designated as membranous web (MW), that harbours this complex. HCV NS4B is an integral membrane protein predicted to comprise four transmembrane segments in its central part. The N‐terminal part comprises two amphipathic α‐helices of which the second has the potential to traverse the membrane bilayer, likely upon oligomerisation. The C‐terminal part comprises a predicted highly conserved α‐helix, a membrane‐associated amphipathic α‐helix and two reported palmitoylation sites. NS4B interacts with other viral nonstructural proteins and has been reported to bind viral RNA. In addition, it was found to harbour an NTPase activity. Finally, NS4B has recently been found to have a role in viral assembly. Much work needs to be done with respect to further dissecting these multiple functions as well as providing a refined membrane topology and complete structure of NS4B. Progress in this direction should yield important insights into the functional architecture of the HCV replication complex and may reveal new opportunities for antiviral intervention against a leading cause of chronic hepatitis, liver cirrhosis and hepatocellular carcinoma worldwide. Copyright © 2010 John Wiley & Sons, Ltd.