TY - JOUR
T1 - Host cell kinases and the hepatitis C virus life cycle
AU - Colpitts, Che C
AU - Lupberger, Joachim
AU - Doerig, Christian D
AU - Baumert, Thomas F
PY - 2015
Y1 - 2015
N2 - Hepatitis C virus (HCV) infection relies on virus-host interactions with human hepatocytes, a context in which host cell kinases play critical roles in every step of the HCV life cycle. During viral entry, cellular kinases, including EGFR, EphA2 and PKA, regulate the localization of host HCV entry factors and induce receptor complex assembly. Following virion internalization, viral genomes replicate on endoplasmic reticulum-derived membranous webs. The formation of membranous webs depends on interactions between the HCV NS5a protein and PI4KIIIalpha. The phosphorylation status of NS5a, regulated by PI4KIIIalpha, CKI and other kinases, also acts as a molecular switch to virion assembly, which takes place on lipid droplets. The formation of lipid droplets is enhanced by HCV activation of IKKalpha. In view of the multiple crucial steps in the viral life cycle that are mediated by host cell kinases, these enzymes also represent complementary targets for antiviral therapy. This article is part of a Special Issue entitled: Inhibitors of Protein Kinases.
AB - Hepatitis C virus (HCV) infection relies on virus-host interactions with human hepatocytes, a context in which host cell kinases play critical roles in every step of the HCV life cycle. During viral entry, cellular kinases, including EGFR, EphA2 and PKA, regulate the localization of host HCV entry factors and induce receptor complex assembly. Following virion internalization, viral genomes replicate on endoplasmic reticulum-derived membranous webs. The formation of membranous webs depends on interactions between the HCV NS5a protein and PI4KIIIalpha. The phosphorylation status of NS5a, regulated by PI4KIIIalpha, CKI and other kinases, also acts as a molecular switch to virion assembly, which takes place on lipid droplets. The formation of lipid droplets is enhanced by HCV activation of IKKalpha. In view of the multiple crucial steps in the viral life cycle that are mediated by host cell kinases, these enzymes also represent complementary targets for antiviral therapy. This article is part of a Special Issue entitled: Inhibitors of Protein Kinases.
UR - http://www.ncbi.nlm.nih.gov/pubmed/25896387
U2 - 10.1016/j.bbapap.2015.04.011
DO - 10.1016/j.bbapap.2015.04.011
M3 - Article
VL - 1854
SP - 1657
EP - 1662
JO - BBA Proteins and Proteomics
JF - BBA Proteins and Proteomics
SN - 1570-9639
IS - 10 [Part B]
ER -