首页 | 本学科首页   官方微博 | 高级检索  
     


Hepatitis C virus NS5A protein modulates template selection by the RNA polymerase in in vitro system
Authors:Alexander V. Ivanov  Vera L. Tunitskaya  Vladimir A. Mitkevich  Vladimir S. Prassolov  Marina K. Kukhanova
Affiliation:a Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Vavilov street, 32, Moscow 119991, Russia
b University of Oslo, Centre for Medical Study in Russia, Moscow 119334, Russia
Abstract:Hepatitis C virus (HCV) NS5A phosphoprotein is a component of virus replicase. Here we demonstrate that in vitro unphosphorylated NS5A protein inhibits HCV RNA-dependent RNA polymerase (RdRp) activity in polyA-oligoU system but has little effect on synthesis of viral RNA. The phosphorylated casein kinase (CK) II NS5A protein causes the opposite effect on RdRp in each of these systems. The phosphorylation of NS5A protein with CKII does not affect its affinity to the HCV RdRp and RNA. The NS5A phosphorylation with CKI does not change the RdRp activity. Herein we report evidence that the NS5A prevents template binding to the RdRp.

Structured summary

MINT-6803697: CKI (uniprotkb:P97633) phosphorylates (MI:0217) NS5A (uniprotkb:P26662) by protein kinase assay (MI:0424)MINT-6803713: CKII (uniprotkb:P67870) phosphorylates (MI:0217) NS5A (uniprotkb:P26662) by protein kinase assay (MI:0424)
Keywords:HCV, hepatitis C virus   RdRp, RNA-dependent RNA polymerase   CK, casein kinase   UTR, untranslated region
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号