Comparative Proteomics Reveals Important Viral-Host Interactions in HCV-Infected Human Liver Cells

PLoS One. 2016 Jan 25;11(1):e0147991. doi: 10.1371/journal.pone.0147991. eCollection 2016.

Abstract

Hepatitis C virus (HCV) poses a global threat to public health. HCV envelop protein E2 is the major component on the virus envelope, which plays an important role in virus entry and morphogenesis. Here, for the first time, we affinity purified E2 complex formed in HCV-infected human hepatoma cells and conducted comparative mass spectrometric analyses. 85 cellular proteins and three viral proteins were successfully identified in three independent trials, among which alphafetoprotein (AFP), UDP-glucose: glycoprotein glucosyltransferase 1 (UGT1) and HCV NS4B were further validated as novel E2 binding partners. Subsequent functional characterization demonstrated that gene silencing of UGT1 in human hepatoma cell line Huh7.5.1 markedly decreased the production of infectious HCV, indicating a regulatory role of UGT1 in viral lifecycle. Domain mapping experiments showed that HCV E2-NS4B interaction requires the transmembrane domains of the two proteins. Altogether, our proteomics study has uncovered key viral and cellular factors that interact with E2 and provided new insights into our understanding of HCV infection.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Validation Study

MeSH terms

  • Glucuronosyltransferase / metabolism
  • HEK293 Cells
  • Hepacivirus / physiology*
  • Host-Pathogen Interactions*
  • Humans
  • Liver / metabolism
  • Liver / virology*
  • Proteomics*
  • Tandem Mass Spectrometry
  • Viral Nonstructural Proteins / metabolism
  • alpha-Fetoproteins / metabolism

Substances

  • NS4B protein, flavivirus
  • Viral Nonstructural Proteins
  • alpha-Fetoproteins
  • Glucuronosyltransferase